Therapeutic Goods Administration · January 1, 2036
- Affected product
- VELA Tango 700E Mobility Chair
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action In chairs manufactured between February 2025 and October 2025 the manufacturer, Vermund Larsen A/S, has identified a defect in the seat tilt actuator which may cause it to fracture during use. This may cause the…
Check affected VELA Tango 700E Mobility Chair identifiers →Therapeutic Goods Administration · September 8, 2028
- Affected product
- Tooth Mousse Plus - Strawberry Flavour
- Category
- Medical device recalls
- Hazard
- Classification Class III Reason for the Action GC Australasia Dental has reported a labelling error regarding the carton (tube box) of Tooth Mousse Plus - Strawberry Flavour. The product is correctly packaged in the Tooth Mousse Plus - Strawberry tube, outer…
Check affected Tooth Mousse Plus - Strawberry Flavour identifiers →Therapeutic Goods Administration · October 20, 2027
- Affected product
- Bravo CF capsule delivery device, 5-pk
- Category
- Medical device recalls
- Hazard
- Classification Class I Reason for the Action Medtronic has identified an increase in complaints involving the Bravo CF capsule delivery device where the capsule fails to attach to the oesophagus or detach from the delivery device. Medtronic's preliminary root…
Check affected Bravo CF capsule delivery device, 5-pk identifiers →Therapeutic Goods Administration · April 30, 2027
- Affected product
- Sundaze Polaris 29% THC Flower 10g Jar
- Category
- Medical device recalls
- Hazard
- Classification Class III Reason for the Action Sundaze Polaris 29% THC Dried Flower 10g Jar primary container labels have an incorrect machine-readable barcode printed on the packaging. The printed barcode duplicates that of Sundaze Apollo (20% THC Dried…
Check affected Sundaze Polaris 29% THC Flower 10g Jar identifiers →Therapeutic Goods Administration · March 31, 2027
- Affected product
- Rua Puawai THC24
- Category
- Medical device recalls
- Hazard
- Classification Class III Reason for the Action Rua Puawai THC24 was intended for supply in the New Zealand market; however, affected stock was supplied in error to two Australian pharmacies in place of Rua Puawai T24. No other batches of Rua Puawai THC24 have…
Check affected Rua Puawai THC24 identifiers →Therapeutic Goods Administration · October 8, 2026
- Affected product
- Imager II Angiographic Catheters
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Boston Scientific is initiating an urgent recall of Imager II Angiographic Catheters due to a manufacturing problem affecting the catheter tip. Boston Scientific has determined that these Catheters were…
Check affected Imager II Angiographic Catheters identifiers →Therapeutic Goods Administration · September 27, 2026
- Affected product
- Irinotecan HCL 206mg In 0.9% Sodium Chloride in Polyolefin Bag
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Upon receipt of compounding product, Irinotecan HCL, the customer has identified a leaking product within the protective inner clear bag. The spill was contained within the bag and deemed not safe for patient use.…
Check affected Irinotecan HCL 206mg In 0.9% Sodium Chloride in Polyolefin Bag identifiers →Therapeutic Goods Administration · August 31, 2026
- Affected product
- CombiDiagnost R90, DigitalDiagnost 4, DigitalDiagnost C90, and
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Following implementation of PSC 10.1, Philips identified several problems affecting DigitalDiagnost and ProxiDiagnost/ CombiDiagnost systems: 1. The system may not enter a ready state for wall stand exposures when…
Check affected CombiDiagnost R90, DigitalDiagnost 4, DigitalDiagnost C90, and identifiers →ACCC Product Safety Australia · August 27, 2026
- Affected product
- Husqvarna Cross Country dirt bikes
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury or death if the brake calliper fails and causes an accident. An incident of the brake calliper failing causing an accident has occurred overseas. What consumers should do Stop using the dirt bike immediately. Do not use the…
Check affected Husqvarna Cross Country dirt bikes identifiers →ACCC Product Safety Australia · August 27, 2026
- Affected product
- Basco BFO-15671 oil filter for diesel engines
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of death, serious injury or property damage (including to other road users) from an accident if the filter loosens or comes off the engine while the vehicle is being driven. The oil spill from the engine may cause a fire if it comes into
Check affected Basco BFO-15671 oil filter for diesel engines identifiers →ACCC Product Safety Australia · August 27, 2026
- Affected product
- GASGAS Motocross and Cross Country motorbikes (MY21-24)
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury or death if the brake calliper fails and causes an accident. An incident of the brake calliper failing causing an accident has occurred overseas. What consumers should do Stop using the dirt bike immediately. Do not use the…
Check affected GASGAS Motocross and Cross Country motorbikes (MY21-24) identifiers →Therapeutic Goods Administration · August 24, 2026
- Affected product
- Dexcom G7 iOS App
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action In G7 iOS App version 2.12, only Critical Alerts are designed to override the phone’s Silent Mode or Focus Mode setting. Non-critical alerts behave in accordance with the phone’s notification settings. In the…
Check affected Dexcom G7 iOS App identifiers →Therapeutic Goods Administration · August 24, 2026
- Affected product
- Dexcom G7 App
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action When in ‘Do Not Disturb’ mode, critical alerts may not vibrate as expected and ‘disk space critical,’ ‘recoverable error,’ and ‘Unrecoverable error’ alerts may not sound or vibrate for up to 25 minutes. If a user…
Check affected Dexcom G7 App identifiers →Therapeutic Goods Administration · August 24, 2026
- Affected product
- Carescape Central Station (CSCS) V3.0.x
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action GE HealthCare has become aware that the Carescape Central Station (CSCS) V3.0.x may not resume patient monitoring for at least 3 minutes following a system restart. This situation can arise only when the ‘Allow…
Check affected Carescape Central Station (CSCS) V3.0.x identifiers →Therapeutic Goods Administration · August 21, 2026
- Affected product
- All GEM PAKs for GEM Premier 5000 with iQM2 and GEM Premier 7000
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Following customer reports, a review of sodium (Na+) results from normal patient populations on the GEM Premier 5000 and GEM Premier 7000 systems shows a negative bias of approximately 3 mmol/L relative to the
Check affected All GEM PAKs for GEM Premier 5000 with iQM2 and GEM Premier 7000 identifiers →Therapeutic Goods Administration · August 21, 2026
- Affected product
- Percussionaire IPV Systems
- Category
- Medical device recalls
- Hazard
- Classification Class I Reason for the Action Percussionaire Corporation has recently received a complaint regarding the use of IPV therapy administered in-line to a mechanically ventilated, sedated patient receiving volatile anaesthetic agents using a…
Check affected Percussionaire IPV Systems identifiers →Therapeutic Goods Administration · August 21, 2026
- Affected product
- Automated Impella Controller (AIC)
- Category
- Medical device recalls
- Hazard
- Classification Class I Reason for the Action Abiomed has identified an increase in complaints due to purge cassette recognition problems resulting from failures of the purge flag component within the purge pressure sensor assembly. The purge flag engages with…
Check affected Automated Impella Controller (AIC) identifiers →ACCC Product Safety Australia · August 21, 2026
- Affected product
- Babybee toddler board with detachable seat
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury to a child from a fall if the detachable seat breaks while in use. Incidents have occurred. What consumers should do Stop using the toddler board immediately and check the batch number on the underside of your Babybee…
Check affected Babybee toddler board with detachable seat identifiers →Therapeutic Goods Administration · August 20, 2026
- Affected product
- Renuvion APR Handpiece
- Category
- Medical device recalls
- Hazard
- Classification Class III Reason for the Action Apyx Medical has updated the labeling for the Renuvion APR Handpieces to align with an update to the intended purpose statement in the Australian Register of Therapeutic Goods (ARTG). To ensure devices supplied to…
Check affected Renuvion APR Handpiece identifiers →ACCC Product Safety Australia · August 20, 2026
- Affected product
- Weet-Bix Wearable Blanket
- Category
- Consumer product recalls
- Hazard
- warning label. The hazards to consumers There is a risk of serious burn injuries if the product is exposed to a heat or flame source. Consumers may not be aware of this risk. What consumers should do Stop using the blanket immediately and place away from heat…
Check affected Weet-Bix Wearable Blanket identifiers →Therapeutic Goods Administration · August 20, 2026
- Affected product
- Clearview, Innovacon, InstAlert and Surestep hCG Tests. An in vitro
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action As part of routine post-market surveillance activities, an investigation was conducted into reports of false-positive results and determined that while the tests demonstrate expected results at and above the…
Check affected Clearview, Innovacon, InstAlert and Surestep hCG Tests. An in vitro identifiers →ACCC Product Safety Australia · August 19, 2026
- Affected product
- ORBEA Optima Asphalt & Comfort e-bikes
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of death, serious injury or property damage (including to other road users) if the bike’s frame breaks while in use and causes an accident. What consumers should do Stop using the bike and check the VIN engraved on the frame. If the bike’s…
Check affected ORBEA Optima Asphalt & Comfort e-bikes identifiers →Therapeutic Goods Administration · August 19, 2026
- Affected product
- Movicol Lemon & Lime 30s, Movicol Chocolate 30s, Movicol Junior
- Category
- Medical device recalls
- Hazard
- Classification Class III Reason for the Action Norgine conducted an investigation into MOVICOL products manufactured using the single-shot campaign filling process utilising residual bulk material which remains in the manufacturing line when an Intermediate…
Check affected Movicol Lemon & Lime 30s, Movicol Chocolate 30s, Movicol Junior identifiers →Therapeutic Goods Administration · August 19, 2026
- Affected product
- S7XTRA 200 Tub Wipes
- Category
- Medical device recalls
- Hazard
- Classification Class III Reason for the Action Dirt and debris have contaminated a small quantity of tubs in Batch: 393253, expiry: 01/2029. The debris appears as small dark spots and smears on the inner sides of the tub and the wipes material. Laboratory…
Check affected S7XTRA 200 Tub Wipes identifiers →Food Standards Australia New Zealand · August 18, 2026
- Affected product
- Chen Foods - Mr Chen's Szechuan Chilli Oil - 250g
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Chen Foods - Mr Chen's Szechuan Chilli Oil - 250g identifiers →Therapeutic Goods Administration · August 18, 2026
- Affected product
- PALACOS R+G pro 40, 60, 80 CE EUR and PALACOS MV+G pro 40, 60, 80 CE
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action There have been isolated cases of monomer liquid leaking from the pro system. Assessments carried out to date have shown that the system can continue to be used as intended. However, if the product does leak, the…
Check affected PALACOS R+G pro 40, 60, 80 CE EUR and PALACOS MV+G pro 40, 60, 80 CE identifiers →ACCC Product Safety Australia · August 18, 2026
- Affected product
- Playground Plus Box 4: Play With Purpose 10-12m toy box
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- to consumers Risk of serious injury or death from choking and asphyxiation if a child places the silicone pull strings in their mouth or if small parts detach from the toy and the child places them in their mouth. What consumers should do Stop using the…
Check affected Playground Plus Box 4: Play With Purpose 10-12m toy box identifiers →ACCC Product Safety Australia · August 18, 2026
- Affected product
- Pull String Interactive Toys
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- to consumers Risk of serious injury or death from choking and asphyxiation if a child places the silicone pull strings in their mouth or if small parts detach from the toy and the child places them in their mouth. What consumers should do Stop using the toy…
Check affected Pull String Interactive Toys identifiers →Food Standards Australia New Zealand · August 18, 2026
- Affected product
- Walter's Artisan Produce Pty Ltd - Walter’s Artisan Bread - Banana
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Walter's Artisan Produce Pty Ltd - Walter’s Artisan Bread - Banana identifiers →Therapeutic Goods Administration · August 18, 2026
- Affected product
- MEDICIANZ MUPIROCIN OINTMENT Mupirocin 2%w/w Tube
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action During ongoing stability testing, an out of specification (OOS) result was obtained for the stability batch (Batch No. S062409.1) at the 24-month testing point for both the assay (content) of Mupirocin and related…
Check affected MEDICIANZ MUPIROCIN OINTMENT Mupirocin 2%w/w Tube identifiers →Therapeutic Goods Administration · August 18, 2026
- Affected product
- iQ200 Series Analyzers and DxU 840m/850m Iris Analyzers. An in vitro
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Beckman Coulter has received customer complaints about lamina fluid leaks in iQ200 Series Analyzers and DxU 840m/850m Iris Analyzers. Investigation determined that the leaks are caused by a check valve in the rinse…
Check affected iQ200 Series Analyzers and DxU 840m/850m Iris Analyzers. An in vitro identifiers →Therapeutic Goods Administration · August 17, 2026
- Affected product
- Various Blood Transfusion Sets, Basic Intravenous Administration
- Category
- Medical device recalls
- Hazard
- Classification Class III Reason for the Action ICU Medical received reports of discolouration observed in the drip chambers of certain IV tubing sets. Instructions for Customers/Users ICU Medical's investigation into the problem confirmed that the observed…
Check affected Various Blood Transfusion Sets, Basic Intravenous Administration identifiers →ACCC Product Safety Australia · August 17, 2026
- Affected product
- Two-stage LPG gas pressure regulator for Snowy River and Newgen
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury or death if the gas leaks near an ignition source and causes an explosion or fire. Risk of serious injury or death by asphyxiation if the leak causes a build-up of gas in an enclosed space. Incidents of the regulator failing…
Check affected Two-stage LPG gas pressure regulator for Snowy River and Newgen identifiers →Therapeutic Goods Administration · August 14, 2026
- Affected product
- Incisive CT and CT 5300 with software version 5.1.2.X
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Philips has identified multiple software problems in software version 5.1.2.X affecting Philips Incisive CT and CT 5300 systems. These problems may affect system performance and result in image reconstruction…
Check affected Incisive CT and CT 5300 with software version 5.1.2.X identifiers →Therapeutic Goods Administration · August 14, 2026
- Affected product
- Hemospray Endoscopic Hemostat
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Cook Medical is updating the Hemospray Instructions for Use (IFU) to include new guidance to address two Hemospray potential problems: 1. Endoscope adhesion and 2. Inability to spray powder. Cook Medical is not…
Check affected Hemospray Endoscopic Hemostat identifiers →Therapeutic Goods Administration · August 14, 2026
- Affected product
- VITROS Chemistry Products VALP Reagent. An in vitro diagnostic
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action QuidelOrtho confirmed a problem involving VITROS Chemistry Products VALP Reagent. Lots from Generations (GENs) 35, 36, and 37 may generate positively biased results. QuidelOrtho’s investigation into the problem…
Check affected VITROS Chemistry Products VALP Reagent. An in vitro diagnostic identifiers →Therapeutic Goods Administration · August 13, 2026
- Affected product
- Portrait Core Services Software version V1.0.5, V1.1 and V1.2
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action GE HealthCare has become aware that during a service event to update Portrait Core Services software at a facility, patients who are monitored on Portrait Mobile devices can be discharged from the Portrait…
Check affected Portrait Core Services Software version V1.0.5, V1.1 and V1.2 identifiers →Therapeutic Goods Administration · August 13, 2026
- Affected product
- Cardioroot Woven Grafts
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Internal testing of samples from CARDIOROOT vascular grafts produced Integral Water Permeability (IWP) results outside the limit specified in the product’s Instructions for Use (IFU) (i.e. Instructions for…
Check affected Cardioroot Woven Grafts identifiers →Food Standards Australia New Zealand · August 13, 2026
- Affected product
- UPDATED 13.08.26 | Edesia Enterprises Pty Ltd T/A noosa GOURMET
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected UPDATED 13.08.26 | Edesia Enterprises Pty Ltd T/A noosa GOURMET identifiers →Therapeutic Goods Administration · August 13, 2026
- Affected product
- Eribulin 1 mg/2 mL Solution for Injection
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Dr. Reddys has identified an out of specification result during stability testing. The assay result reported (93.3 %) is below the registered specification of 95 -100%. Patients receiving this product may be…
Check affected Eribulin 1 mg/2 mL Solution for Injection identifiers →Therapeutic Goods Administration · August 12, 2026
- Affected product
- Adaptable Beach Chair Positioning Kit
- Category
- Medical device recalls
- Hazard
- Classification Class I Reason for the Action Quantum OPS Adaptable Beach Chair Positioning Kits may be affected by a fracture of a welded joint below the patient headrest. The affected welded joint provides structural support for the patient headrest. The…
Check affected Adaptable Beach Chair Positioning Kit identifiers →Food Standards Australia New Zealand · August 12, 2026
- Affected product
- Food alerts
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Food alerts identifiers →Food Standards Australia New Zealand · August 12, 2026
- Affected product
- Edesia Enterprises Pty Ltd T/A noosa GOURMET - Brioche Rolls - 320g
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Edesia Enterprises Pty Ltd T/A noosa GOURMET - Brioche Rolls - 320g identifiers →ACCC Product Safety Australia · August 12, 2026
- Affected product
- Nevenka Baby pull string giraffe toy
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- to consumers Risk of serious injury or death from choking and asphyxiation if a child places the silicone pull strings in their mouth or the feet detach from the toy’s pull strings and the child places them in their mouth. What consumers should do Stop using…
Check affected Nevenka Baby pull string giraffe toy identifiers →Therapeutic Goods Administration · August 11, 2026
- Affected product
- Orthopaedic implant components manufactured from ultra-high
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Certain orthopaedic implants were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five (5) years. Industry guidance for storage duration of UHMWPE raw material…
Check affected Orthopaedic implant components manufactured from ultra-high identifiers →Therapeutic Goods Administration · August 11, 2026
- Affected product
- POWERSEAL 5 MM (in diameter) 23 CM (long) Curved Jaw Sealer &
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Lot FR490902 may contain a labelling discrepancy. Specifically, the affected units were packaged in an outer shelf box labelled for a 37cm device versus an outer shelf box labelled for a 23cm device. However, other…
Check affected POWERSEAL 5 MM (in diameter) 23 CM (long) Curved Jaw Sealer & identifiers →Therapeutic Goods Administration · August 10, 2026
- Affected product
- Azurion R2.x.10, R3.0, R3.1 and R4.0 systems
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Philips has identified 2 potential problems that may lead to delay of therapy, procedural complications and/or inappropriate treatment. • Problem 1: Image quality degradation A problem associated with the Flat…
Check affected Azurion R2.x.10, R3.0, R3.1 and R4.0 systems identifiers →Therapeutic Goods Administration · August 7, 2026
- Affected product
- StrykeFlow PS and AHTO Tube Sets
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action There has been an increase in reported complaints describing leaking from the device during use. During use, the device may experience fluid leakage from the handpiece, which may result in fluid accumulating on the…
Check affected StrykeFlow PS and AHTO Tube Sets identifiers →Therapeutic Goods Administration · August 7, 2026
- Affected product
- Pertuzumab 420mg in 0.9% Sodium Chloride in Polyolefin Bag
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Cairns Hospital reported on 11/08/2026 that a Pertuzumab infusion bag (BB26084718) had expired prior to treatment. The single dose unit had expired during transit to the customer. The customer advised the single…
Check affected Pertuzumab 420mg in 0.9% Sodium Chloride in Polyolefin Bag identifiers →Therapeutic Goods Administration · August 6, 2026
- Affected product
- Meisinger Polishing 2 Step DPO02 204 040 / 2
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Surface cracks of varying severity may occur in the affected polishers. Depending on their extent, these cracks may be visible to different degrees and may impair the mechanical stability of the instrument.…
Check affected Meisinger Polishing 2 Step DPO02 204 040 / 2 identifiers →ACCC Product Safety Australia · August 6, 2026
- Affected product
- True Blue robotic pool cleaner sold at Bunnings Warehouse
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury or death and property damage if the cleaner ignites and causes a fire. Incidents of the cleaner catching fire while charging have occurred. What consumers should do Stop using the robotic pool cleaner immediately. Unplug it…
Check affected True Blue robotic pool cleaner sold at Bunnings Warehouse identifiers →ACCC Product Safety Australia · August 6, 2026
- Affected product
- Findon Light Up Sensory Plush
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious burn injury and property damage if the toy overheats or catches fire while in use. Incidents of overheating have occurred. What consumers should do Stop using the toy immediately, remove the AA batteries and place out of reach of…
Check affected Findon Light Up Sensory Plush identifiers →Food Standards Australia New Zealand · August 5, 2026
- Affected product
- Key-Sun Kids Honey & Eucalyptus + acerola lozenge - 54 g (12 x 4.5 g
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Key-Sun Kids Honey & Eucalyptus + acerola lozenge - 54 g (12 x 4.5 g identifiers →Therapeutic Goods Administration · August 5, 2026
- Affected product
- WaveWriter Alpha Spinal Cord Stimulation (SCS) System
- Category
- Medical device recalls
- Hazard
- Classification Class III Reason for the Action Boston Scientific is notifying customers of an update to the Information for Prescribers and Information for Patients manuals used in Australia for applicable Boston Scientific WaveWriter Alpha Spinal Cord…
Check affected WaveWriter Alpha Spinal Cord Stimulation (SCS) System identifiers →Therapeutic Goods Administration · August 5, 2026
- Affected product
- Craft Botanics White Runtz T25 10g Jar (Dried Herb)
- Category
- Medical device recalls
- Hazard
- Classification Class III Reason for the Action A labelling error has been identified for a specific batch of Craft Botanics White Runtz, following a customer complaint about a different organoleptic profile (appearance and aroma) compared to previous batches.…
Check affected Craft Botanics White Runtz T25 10g Jar (Dried Herb) identifiers →ACCC Product Safety Australia · August 5, 2026
- Affected product
- Secret diary pen with UV light
- Category
- Consumer product recalls
- Hazard
- to consumers Children are at risk of choking, serious injury or death if they swallow or place button/coin batteries inside their bodies. If you suspect a child has swallowed or inserted a button/coin battery: Call Triple Zero (000) if your child is bleeding…
Check affected Secret diary pen with UV light identifiers →Therapeutic Goods Administration · August 4, 2026
- Affected product
- Fludeoxyglucose (18F) Injection (FDG)
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action It was identified there was a discrepancy of the recorded activity and volume supplied on the QC Release Forms than the actual activity and volume supplied in the customer vials. As such, the vials may not have met…
Check affected Fludeoxyglucose (18F) Injection (FDG) identifiers →Therapeutic Goods Administration · August 4, 2026
- Affected product
- Percutaneous Insertion Kits (PIK)
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action It was identified that there have been failures in sterile barrier integrity verification testing. As these failures were not previously addressed in accordance with packaging verification requirements, the…
Check affected Percutaneous Insertion Kits (PIK) identifiers →Therapeutic Goods Administration · August 3, 2026
- Affected product
- LATITUDE Clarity Server Software
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action There is a potential for a delay in AF Burden Alert notification affecting the LATITUDE Clarity server software which supports the LUX-Dx family of ICMs. This delayed AF Burden Alert notification behaviour by…
Check affected LATITUDE Clarity Server Software identifiers →ACCC Product Safety Australia · August 3, 2026
- Affected product
- Jollybaby baby sensory pull string toy whale
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- to consumers Risk of serious injury or death from choking if small parts detach from the toy and the child places them in their mouth. What consumers should do Stop using the toy immediately and place out of reach of children. Cut the strings of the toy and…
Check affected Jollybaby baby sensory pull string toy whale identifiers →Therapeutic Goods Administration · August 3, 2026
- Affected product
- OPTIRAY 350 Ioversol 74% w/v 74.1g/100mL Injection Vial
- Category
- Medical device recalls
- Hazard
- Classification Class III Reason for the Action The vial label of some batches of Optiray 350 100 mL vials is incorrect. It lists the ingredients' quantities for Optiray 350 75 mL vial instead. The ingredients' quantities listed on the product carton are…
Check affected OPTIRAY 350 Ioversol 74% w/v 74.1g/100mL Injection Vial identifiers →Therapeutic Goods Administration · August 3, 2026
- Affected product
- XScribe Cardiac Stress Testing System
- Category
- Medical device recalls
- Hazard
- Classification Class III Reason for the Action Some Q-Stress and XScribe systems experience a problem with the Windows 11 image installed on affected computers. Users may observe a Windows system warning message upon startup that prevents the installation of…
Check affected XScribe Cardiac Stress Testing System identifiers →Therapeutic Goods Administration · August 3, 2026
- Affected product
- GS1-HT Extraction Script for use within EasyScreen Sample Processing
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action The impacted extraction scripts contain a missing section of error-handling code for sample positions 81–95. If a low-volume or missing-sample condition occurs in positions 81 - 95, the script may apply recovery…
Check affected GS1-HT Extraction Script for use within EasyScreen Sample Processing identifiers →Therapeutic Goods Administration · July 31, 2026
- Affected product
- GYNECARE TVT EXACT Continence System
- Category
- Medical device recalls
- Hazard
- Classification Class III Reason for the Action The manufacturer, Ethicon SARL, has identified a problem whereby white particulates were observed within the sterile barrier of certain LOTs. The manufacturer has determined that the white particulates originated…
Check affected GYNECARE TVT EXACT Continence System identifiers →ACCC Product Safety Australia · July 31, 2026
- Affected product
- Pokémon Pikachu Co-BOLT teapot
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious burn injuries and laceration from sharp edges if the teapot cracks or breaks. Incidents of the teapot cracking during use have occurred, with one reported burn injury. What consumers should do Stop using the teapot immediately.…
Check affected Pokémon Pikachu Co-BOLT teapot identifiers →ACCC Product Safety Australia · July 31, 2026
- Affected product
- Glow Crown Headbands with LED battery pack
- Category
- Consumer product recalls
- Hazard
- to consumers Children are at risk of choking, serious injury or death if they swallow or place button or coin batteries inside their bodies. If you suspect a child has swallowed or inserted a button or coin battery: Call Triple Zero (000) if your child is…
Check affected Glow Crown Headbands with LED battery pack identifiers →Therapeutic Goods Administration · July 31, 2026
- Affected product
- Mindray Monitors
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Mindray has identified that certain monitor manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions. To improve clarity and ensure…
Check affected Mindray Monitors identifiers →ACCC Product Safety Australia · July 30, 2026
- Affected product
- Aussie Clean Drain Cleaner 4pk
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious illness or death if a child swallows the contents of the product. Risk of serious injury if the product comes into
Check affected Aussie Clean Drain Cleaner 4pk identifiers →Food Standards Australia New Zealand · July 30, 2026
- Affected product
- UPDATED 30.07.26 | Auxico (Perth) Pty Ltd - LGM HOT CHILLI OIL 275G
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected UPDATED 30.07.26 | Auxico (Perth) Pty Ltd - LGM HOT CHILLI OIL 275G identifiers →Therapeutic Goods Administration · July 30, 2026
- Affected product
- Beckman Coulter Chemistry Analyzer AU480. An in vitro diagnostic
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Beckman Coulter has determined that CHEMISTRY ANALYZER AU480 with Windows 10 IoT Enterprise 2021 LTSC PCs listed above may output the message “System Stopped By Fatal Error: DBConnectionError AlarmDB when launching…
Check affected Beckman Coulter Chemistry Analyzer AU480. An in vitro diagnostic identifiers →Therapeutic Goods Administration · July 29, 2026
- Affected product
- High Filtration Surgical Face Masks with Ties Level 3
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action The Therapeutic Goods Administration (TGA) conducted a post-market review of face masks included in the Australian Register of Therapeutic Goods (ARTG). Med-Con Pty Ltd was found to have supplied four batches of…
Check affected High Filtration Surgical Face Masks with Ties Level 3 identifiers →Therapeutic Goods Administration · July 29, 2026
- Affected product
- SACRO Sacrocolpopexy Tips
- Category
- Medical device recalls
- Hazard
- Classification Class III Reason for the Action Certain LOTs were assembled with an internal hub in the incorrect orientation. The inverted assembly prevents the tip from being attached to the compatible RUMI system or Advincula Arch handle. If the SACRO…
Check affected SACRO Sacrocolpopexy Tips identifiers →ACCC Product Safety Australia · July 28, 2026
- Affected product
- The Dot Space laser cat toy
- Category
- Baby product recalls, Pet food recalls, Consumer product recalls
- Hazard
- to consumers Children are at risk of choking, serious injury or death if they swallow or place button/coin batteries inside their bodies. If you suspect a child has swallowed or inserted a button/coin battery: Call Triple Zero (000) if your child is bleeding…
Check affected The Dot Space laser cat toy identifiers →ACCC Product Safety Australia · July 28, 2026
- Affected product
- Crazer LED light show toy - 5 Images
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- to consumers Children are at risk of choking, serious injury or death if they swallow or place button/coin batteries inside their bodies. If you suspect a child has swallowed or inserted a button/coin battery: Call Triple Zero (000) if your child is bleeding…
Check affected Crazer LED light show toy - 5 Images identifiers →Therapeutic Goods Administration · July 28, 2026
- Affected product
- GORE EXCLUDER Thoracoabdominal Branch Endoprosthesis (TAMBE)
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Following a request from the US FDA to update the Instructions for Use (IFU) for the GORE EXCLUDER Thoracoabdominal Branch Endoprosthesis (TAMBE) during its review of the TAMBE 2026 IDE Annual Report (G150071/R061)…
Check affected GORE EXCLUDER Thoracoabdominal Branch Endoprosthesis (TAMBE) identifiers →ACCC Product Safety Australia · July 28, 2026
- Affected product
- ARB bull bar mounting brackets for MY26 N90 Hilux
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury or property damage (including to other road users) if the bull bar detaches from the vehicle. An incident of the bull bar detaching has occurred. What consumers should do Stop using the vehicle on corrugated roads…
Check affected ARB bull bar mounting brackets for MY26 N90 Hilux identifiers →Therapeutic Goods Administration · July 27, 2026
- Affected product
- Neoss Guide Implant Inserters
- Category
- Medical device recalls
- Hazard
- Classification Class III Reason for the Action The guide inserters were produced with incorrect laser marking. The physical product is showing ‘S SP’. The correct platform ‘N NP’ is identified on the product label. The incorrect laser marking could potentially…
Check affected Neoss Guide Implant Inserters identifiers →Therapeutic Goods Administration · July 27, 2026
- Affected product
- MicroVue SC5b-9 Plus EIA. An in vitro diagnostic medical device
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action QuidelOrtho received complaints about discrepancies in patient correlation results with percent differences compared to the previous lot. We have confirmed a high bias between samples from the previous lot and lot…
Check affected MicroVue SC5b-9 Plus EIA. An in vitro diagnostic medical device identifiers →Therapeutic Goods Administration · July 27, 2026
- Affected product
- Fludeoxyglucose (18F) Injection (FDG)
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Cyclotek was notified of a defective product (cracked vial), that was supplied to a customer site on 27 July 2026. The defect was identified upon receipt and was returned to the manufacturing facility. A new vial…
Check affected Fludeoxyglucose (18F) Injection (FDG) identifiers →Therapeutic Goods Administration · July 26, 2026
- Affected product
- Bendamustine HCL 159mg in 0.9% Sodium Chloride in Polyolefin Bag
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Upon receipt of compounded product, Bendamustine, the customer has identified a leaking product within the protective inner clear bag. The spill was contained within the bag and deemed not safe for patient use. The…
Check affected Bendamustine HCL 159mg in 0.9% Sodium Chloride in Polyolefin Bag identifiers →Food Standards Australia New Zealand · July 24, 2026
- Affected product
- Yumbah Aquaculture Ltd - Yumbah Australian Greenlip Abalone 1kg
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Yumbah Aquaculture Ltd - Yumbah Australian Greenlip Abalone 1kg identifiers →Food Standards Australia New Zealand · July 24, 2026
- Affected product
- Food templates
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Food templates identifiers →ACCC Product Safety Australia · July 24, 2026
- Affected product
- Mondraker ONOFF S9 carbon MTB handlebar
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury or death if the handlebar cracks or breaks and causes a rider to lose control of the bicycle and fall. Incidents of the handlebar breaking have occurred. What consumers should do Stop using the affected bicycle immediately.…
Check affected Mondraker ONOFF S9 carbon MTB handlebar identifiers →Food Standards Australia New Zealand · July 24, 2026
- Affected product
- Viet Meatballs - Chinese Sausage - 500g
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Viet Meatballs - Chinese Sausage - 500g identifiers →Therapeutic Goods Administration · July 24, 2026
- Affected product
- Fludeoxyglucose (18F) Injection (FDG)
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Batch FDG260724A failed sterility result due to the presence of Lederbergia (Bacillus) sp at 14 days of incubation. Given the nature of the product, this action was undertaken prior to TGA notification (Immediate…
Check affected Fludeoxyglucose (18F) Injection (FDG) identifiers →ACCC Product Safety Australia · July 24, 2026
- Affected product
- Scented wood bowl & coconut bowl candles
- Category
- Consumer product recalls
- Hazard
- The hazards to consumers Risk of serious injury or death from burns and/or property damage if the candle catches fire. What consumers should do Stop using the candle immediately and place it away from any ignition source.
Check affected Scented wood bowl & coconut bowl candles identifiers →ACCC Product Safety Australia · July 23, 2026
- Affected product
- XTM TTF fridge freezer range
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury, death or property damage if the product catches fire. What consumers should do Stop using the product immediately. Return the product to your nearest store of purchase for a full refund.
Check affected XTM TTF fridge freezer range identifiers →ACCC Product Safety Australia · July 22, 2026
- Affected product
- Krabooz Temperature Gauge & Hydrometer
- Category
- Consumer product recalls
- Hazard
- to consumers Children are at risk of choking, severe internal burn injuries or death if they swallow or place button or coin batteries inside their bodies. Serious injury can occur in as little as 2 hours and the results can be fatal. In Australia, children…
Check affected Krabooz Temperature Gauge & Hydrometer identifiers →ACCC Product Safety Australia · July 22, 2026
- Affected product
- Insectimo hygrometer
- Category
- Consumer product recalls
- Hazard
- to consumers Children are at risk of choking, severe internal burn injuries or death if they swallow or place button or coin batteries inside their bodies. Serious injury can occur in as little as 2 hours and the results can be fatal. In Australia, children…
Check affected Insectimo hygrometer identifiers →Food Standards Australia New Zealand · July 17, 2026
- Affected product
- Truong Ton Group - Vietnamese Sausage 500g
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Truong Ton Group - Vietnamese Sausage 500g identifiers →ACCC Product Safety Australia · July 15, 2026
- Affected product
- Trione in-desk power hub
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury, death and/or property damage from fire or electric shock. Incidents have occurred. What consumers should do 1. Stop using
Check affected Trione in-desk power hub identifiers →ACCC Product Safety Australia · July 15, 2026
- Affected product
- Galmet ColdGal Brushable Paint
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury or irritation, particularly to the eyes, from exposure to paint if it expels from the container under pressure when it is opened. An incident has occurred. What consumers should do Stop using the product immediately and…
Check affected Galmet ColdGal Brushable Paint identifiers →ACCC Product Safety Australia · July 15, 2026
- Affected product
- Essex, Maxim and Sierra electric recliners and sofas with heat pads
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury, death and/or property damage from the heat pads overheating or catching fire while in use. Incidents have occurred. What consumers should do Stop using the heat pad function immediately and disconnect the sofa or recliner…
Check affected Essex, Maxim and Sierra electric recliners and sofas with heat pads identifiers →ACCC Product Safety Australia · July 14, 2026
- Affected product
- Toe warmers 2pk
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious burn injuries and irritation to the skin or eyes if the product overheats or bursts while in use. Incidents of the warmer overheating and bursting have occurred. What consumers should do Stop using the product immediately and keep…
Check affected Toe warmers 2pk identifiers →Food Standards Australia New Zealand · July 14, 2026
- Affected product
- Tasmanian Mountain Waters Exp - Mt Ossa Australian Spring Water
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Tasmanian Mountain Waters Exp - Mt Ossa Australian Spring Water identifiers →ACCC Product Safety Australia · July 13, 2026
- Affected product
- Toy Story 5 Collector Cup and Topper
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- for young children. The hazards to consumers Risk of serious injury or death from choking if the topper breaks into small pieces and a child swallows it. What consumers should do Stop using the cup and topper immediately and keep out of reach of children.…
Check affected Toy Story 5 Collector Cup and Topper identifiers →ACCC Product Safety Australia · July 10, 2026
- Affected product
- Fotopro Bluetooth smartphone shutter remote
- Category
- Consumer product recalls
- Hazard
- to consumers Children are at risk of choking, severe internal burn injuries or death if they swallow or place button/coin batteries inside their bodies. Serious injury can occur in as little as 2 hours and the results can be fatal. In Australia, children have…
Check affected Fotopro Bluetooth smartphone shutter remote identifiers →Food Standards Australia New Zealand · July 10, 2026
- Affected product
- Snackbrands Australia - Chickadees Various Sizes
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Snackbrands Australia - Chickadees Various Sizes identifiers →ACCC Product Safety Australia · July 10, 2026
- Affected product
- Nuby Foldable Bathtub for babies and infants
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- to consumers Risk of serious injury or death from drowning if the product is not used as intended. What consumers should do Stop using the bathtub immediately. Return to an ALDI store for a full refund.
Check affected Nuby Foldable Bathtub for babies and infants identifiers →ACCC Product Safety Australia · July 9, 2026
- Affected product
- Think, Feel, Do Sensory Bear
- Category
- Consumer product recalls
- Hazard
- to consumers There is a risk of serious injury or death by choking if small pellets are released from the toy and a child places them in their mouth. An incident of seam failure has occurred. What consumers should do Stop using the bear immediately and place…
Check affected Think, Feel, Do Sensory Bear identifiers →Food Standards Australia New Zealand · July 9, 2026
- Affected product
- La Vera Group Pty Ltd- La Vera Cheddar Pepper R/W approx 300g
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected La Vera Group Pty Ltd- La Vera Cheddar Pepper R/W approx 300g identifiers →ACCC Product Safety Australia · July 7, 2026
- Affected product
- The 2026 $2 Uncirculated Coin – Tooth Fairy Kit
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of irritation or injury if the chemical odour is inhaled. What consumers should do Stop using the product immediately and keep out of reach of children. Return the product to the place of purchase for a full refund or a replacement product.…
Check affected The 2026 $2 Uncirculated Coin – Tooth Fairy Kit identifiers →Food Standards Australia New Zealand · July 7, 2026
- Affected product
- UPDATED 07.07.2026 | Bellevue Orchard Pty Ltd - Summer Snow - Pink
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected UPDATED 07.07.2026 | Bellevue Orchard Pty Ltd - Summer Snow - Pink identifiers →Food Standards Australia New Zealand · July 6, 2026
- Affected product
- State and territory food action officers
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected State and territory food action officers identifiers →Therapeutic Goods Administration · July 3, 2026
- Affected product
- Panocell 16. An in vitro diagnostic medical device (IVD)
- Category
- Medical device recalls
- Hazard
- Classification Class III Reason for the Action Antibody identification testing performed with Donor B11752 (cell 11 of lot 17453/17453Z) may show positive reactions in the presence of Anti-P1, while the negative antigen from the master list would suggest a…
Check affected Panocell 16. An in vitro diagnostic medical device (IVD) identifiers →Food Standards Australia New Zealand · June 30, 2026
- Affected product
- Kaisi Melbourne Pty Ltd - Wu Xian Zhai Soybean Snacks - Five Spice
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Kaisi Melbourne Pty Ltd - Wu Xian Zhai Soybean Snacks - Five Spice identifiers →Food Standards Australia New Zealand · June 17, 2026
- Affected product
- UPDATED 17.06.26 | ASO United Pty Ltd - Cooked Scampi Shrimp Head-On
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected UPDATED 17.06.26 | ASO United Pty Ltd - Cooked Scampi Shrimp Head-On identifiers →Food Standards Australia New Zealand · June 11, 2026
- Affected product
- Mama Nayture Pty Ltd - Drink Purple 60ml and 350ml
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Mama Nayture Pty Ltd - Drink Purple 60ml and 350ml identifiers →Therapeutic Goods Administration · June 5, 2026
- Affected product
- Stella 2.0 Implant Orientation Diagram (IOD) Incorrect Axis
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action STAAR Surgical has become aware that a limited number of IODs generated have the risk of an IOD with an incorrect axis value that could be clinically significant. Specifically, per the review of data in Stella 2.0,…
Check affected Stella 2.0 Implant Orientation Diagram (IOD) Incorrect Axis identifiers →Food Standards Australia New Zealand · June 2, 2026
- Affected product
- Nestle Australia Ltd. - Allen's iNSiDE OUTS - 130g
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Nestle Australia Ltd. - Allen's iNSiDE OUTS - 130g identifiers →Food Standards Australia New Zealand · May 19, 2026
- Affected product
- Global Seafood Distributors (Australia) Pty Ltd - Seafood Marinara
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Global Seafood Distributors (Australia) Pty Ltd - Seafood Marinara identifiers →Food Standards Australia New Zealand · May 13, 2026
- Affected product
- Murray River Smokehouse - Turkey Bacon - 150g
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Murray River Smokehouse - Turkey Bacon - 150g identifiers →Food Standards Australia New Zealand · May 5, 2026
- Affected product
- Han Yang Import & Export Pty Ltd T/A ByAsia Food - The Han Kitchen
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Han Yang Import & Export Pty Ltd T/A ByAsia Food - The Han Kitchen identifiers →Food Standards Australia New Zealand · May 1, 2026
- Affected product
- Planet Organic Garlic Powder 50g – Certified Organic
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Planet Organic Garlic Powder 50g – Certified Organic identifiers →Food Standards Australia New Zealand · April 30, 2026
- Affected product
- Concordia Traders (Aust) Pty Ltd - Enoki Mushroom 350g
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Concordia Traders (Aust) Pty Ltd - Enoki Mushroom 350g identifiers →Therapeutic Goods Administration · April 29, 2026
- Affected product
- Fertilisation Medium FEM-50
- Category
- Medical device recalls
- Hazard
- Classification Class III Reason for the Action The endotoxin testing method has changed due to the end of life of the testing kits used by Genea Biomedx for quantifying endotoxin levels. The Instructions for Use (IFU) was not updated to remove the mention of…
Check affected Fertilisation Medium FEM-50 identifiers →Food Standards Australia New Zealand · April 24, 2026
- Affected product
- Gold Coast Baking -King Henrys Bakehouse Rye Bread - 900g
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Gold Coast Baking -King Henrys Bakehouse Rye Bread - 900g identifiers →Food Standards Australia New Zealand · April 21, 2026
- Affected product
- Greenstorm Foods t/a Austral Herbs- Certified Organic Garlic Powder
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Greenstorm Foods t/a Austral Herbs- Certified Organic Garlic Powder identifiers →Food Standards Australia New Zealand · April 20, 2026
- Affected product
- Ministry of Chocolate Pty Ltd – NEW YORK INSPIRED - 195g
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Ministry of Chocolate Pty Ltd – NEW YORK INSPIRED - 195g identifiers →Food Standards Australia New Zealand · April 2, 2026
- Affected product
- Coffee Works - Various Chocolate Products
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Coffee Works - Various Chocolate Products identifiers →Food Standards Australia New Zealand · March 31, 2026
- Affected product
- Natural Raw C Pty Ltd - Raw C Easter Coconut Water - 1L
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Natural Raw C Pty Ltd - Raw C Easter Coconut Water - 1L identifiers →Food Standards Australia New Zealand · March 26, 2026
- Affected product
- Loco Love Pty Ltd - Classic Chewy Caramel 5 Pack - 175g
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Loco Love Pty Ltd - Classic Chewy Caramel 5 Pack - 175g identifiers →Food Standards Australia New Zealand · March 24, 2026
- Affected product
- Barkly Smokehouse Pty Ltd - Lux Ham 1.9 kg
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Barkly Smokehouse Pty Ltd - Lux Ham 1.9 kg identifiers →Therapeutic Goods Administration · November 4, 2025
- Affected product
- Getinge Assured Batch Monitoring PCD
- Category
- Medical device recalls
- Hazard
- Classification Class III Reason for the Action Getinge has identified a problem with certain Getinge Assured Batch Monitoring PCD units, where the required O-ring was not installed during manufacture following a customer complaint. The root cause was…
Check affected Getinge Assured Batch Monitoring PCD identifiers →Food Standards Australia New Zealand · October 27, 2025
- Affected product
- FAQs for food businesses
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected FAQs for food businesses identifiers →Food Standards Australia New Zealand · June 26, 2025
- Affected product
- Food incidents
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Food incidents identifiers →Food Standards Australia New Zealand · March 13, 2025
- Affected product
- About food
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected About food identifiers →Food Standards Australia New Zealand · February 25, 2025
- Affected product
- How to food
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected How to food identifiers →Food Standards Australia New Zealand · February 25, 2025
- Affected product
- Food Industry Protocol
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Food Industry Protocol identifiers →Therapeutic Goods Administration · September 16, 2024
- Affected product
- BIOFIRE FILMARRAY TORCH System Base. An in vitro diagnostic medical
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Power cycling can lead to arcing inside of the power switch and may result in carbon build-up and/or deformation of the power switch case. Carbon build-up and/or deformation may result in an open circuit causing…
Check affected BIOFIRE FILMARRAY TORCH System Base. An in vitro diagnostic medical identifiers →Therapeutic Goods Administration · July 26, 2024
- Affected product
- McGRATH MAC video laryngoscope
- Category
- Medical device recalls
- Hazard
- Classification Class I Reason for the Action Medtronic have reported that the battery management system within the devices being removed (McGRATH MAC EMS Video Laryngoscope device, catalogue number 300-200-000; supplied under Stryker Catalogue number…
Check affected McGRATH MAC video laryngoscope identifiers →Therapeutic Goods Administration · September 4, 2019
- Affected product
- Steam Sterilizers with vertical moving doors
- Category
- Medical device recalls
- Hazard
- Classification Class II Reason for the Action Getinge Sterilization AB received a report of a user injury involving the autoclave door. The sterilisation technician activated the door lock while a basket was obstructing the door’s movement. Rather than…
Check affected Steam Sterilizers with vertical moving doors identifiers →Food Standards Australia New Zealand · January 1, 2016
- Affected product
- Food statistics
- Category
- Food recalls
- Hazard
- assessment process and certification Requirements for the importation of beef and beef products for human consumption Exporting beef or beef products to Australia Frequently asked questions (BSE) Status of country BSE food safety risk assessments Australian…
Check affected Food statistics identifiers →