Food Standards Australia New Zealand · August 18, 2026
- Affected product
- UPDATED 02.09.26 | Walter's Artisan Produce Pty Ltd - Walter’s
- Category
- Food recalls
- Hazard
- Any consumers who have an egg allergy or intolerance may have a reaction if the product is consumed.
Check affected UPDATED 02.09.26 | Walter's Artisan Produce Pty Ltd - Walter’s identifiers →Therapeutic Goods Administration · August 18, 2026
- 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 · 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 →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 →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 →Food Standards Australia New Zealand · August 12, 2026
- Affected product
- UPDATED 13.08.26 | Edesia Enterprises Pty Ltd T/A noosa GOURMET
- Category
- Food recalls
- Hazard
- Any consumers who have an egg or milk allergy or intolerance may have a reaction if the product is consumed.
Check affected UPDATED 13.08.26 | Edesia Enterprises Pty Ltd T/A noosa GOURMET identifiers →Food Standards Australia New Zealand · August 12, 2026
- Affected product
- UPDATED 13.08.26 | Edesia Enterprises Pty Ltd T/A noosa GOURMET
- Category
- Food recalls
- Hazard
- Any consumers who have an egg or milk allergy or intolerance may have a reaction if the product is consumed.
Check affected UPDATED 13.08.26 | Edesia Enterprises Pty Ltd T/A noosa GOURMET 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 →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
- 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 · 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
- Food products containing metal may cause injury if consumed.
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 →
