ACCC Product Safety Australia · September 1, 2026
- Affected product
- ISC REFLEX mechanical hitch climbing device
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury or death from falling if the mechanical hitch slips while in use. Incidents have occurred. What consumers should do Stop using ISC REFLEX mechanical hitches immediately. Return affected ISC REFLEX hitches to LRV8 Rescue with…
Check affected ISC REFLEX mechanical hitch climbing device identifiers →Therapeutic Goods Administration · September 1, 2026
- Affected product
- Artisan Link Pro and Artisan Link System. An in vitro diagnostic
- Category
- Medical device recalls
- Hazard
- 1/09/2026 Artisan Link Pro and Artisan Link System. An in vitro diagnostic medical device (IVD). Medical Device Product Alert Class II Hospital
Check affected Artisan Link Pro and Artisan Link System. An in vitro diagnostic identifiers →Therapeutic Goods Administration · September 1, 2026
- Affected product
- Trinity Biotech Oxalate Reagent B and Oxalate Kit. An in vitro
- Category
- Medical device recalls
- Hazard
- 1/09/2026 Trinity Biotech Oxalate Reagent B and Oxalate Kit. An in vitro diagnostic medical device (IVD) Medical Device Recall Class II Hospital
Check affected Trinity Biotech Oxalate Reagent B and Oxalate Kit. An in vitro identifiers →Therapeutic Goods Administration · August 31, 2026
- Affected product
- D-100 Hemoglobin A1c Analytical Calibrator/Cartridge Pack. An in
- Category
- Medical device recalls
- Hazard
- 31/08/2026 D-100 Hemoglobin A1c Analytical Calibrator/Cartridge Pack. An in vitro diagnostic medical device (IVD). Medical Device Product Alert Class II Hospital
Check affected D-100 Hemoglobin A1c Analytical Calibrator/Cartridge Pack. An in 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 →Therapeutic Goods Administration · August 31, 2026
- Affected product
- Liquid Urine Control and Liquid Assayed Chemistry Control Premium
- Category
- Medical device recalls
- Hazard
- 31/08/2026 Liquid Urine Control and Liquid Assayed Chemistry Control Premium Plus. An in vitro diagnostic medical device (IVD) Medical Device Product Correction Class II Hospital
Check affected Liquid Urine Control and Liquid Assayed Chemistry Control Premium identifiers →Therapeutic Goods Administration · August 31, 2026
- Affected product
- Atellica CH Revised C Reactive Protein (RCRP). An in vitro
- Category
- Medical device recalls
- Hazard
- 31/08/2026 Atellica CH Revised C Reactive Protein (RCRP). An in vitro diagnostic medical device (IVD) Medical Device Product Correction Class III Hospital
Check affected Atellica CH Revised C Reactive Protein (RCRP). An in vitro identifiers →Therapeutic Goods Administration · August 28, 2026
- Affected product
- Imaging Ring
- Category
- Medical device recalls
- Hazard
- 28/08/2026 Imaging Ring Medical Device Product Correction Class II Hospital
Check affected Imaging Ring identifiers →Therapeutic Goods Administration · August 28, 2026
- Affected product
- Philips iCT, Ingenuity CT, and Brilliance CT 64 and IQon Spectral CT
- Category
- Medical device recalls
- Hazard
- 28/08/2026 Philips iCT, Ingenuity CT, and Brilliance CT 64 and IQon Spectral CT systems Medical Device Product Correction Class II Hospital
Check affected Philips iCT, Ingenuity CT, and Brilliance CT 64 and IQon Spectral CT identifiers →Therapeutic Goods Administration · August 28, 2026
- Affected product
- Shiley Hi-Lo Evac Cuffed Tracheostomy Tubes supplied with a Hi-Lo
- Category
- Medical device recalls
- Hazard
- 28/08/2026 Shiley Hi-Lo Evac Cuffed Tracheostomy Tubes supplied with a Hi-Lo cuff, standard 15 mm connector, obturator (where applicable), and tape tie. Medical Device Recall Class I Hospital
Check affected Shiley Hi-Lo Evac Cuffed Tracheostomy Tubes supplied with a Hi-Lo identifiers →Therapeutic Goods Administration · August 27, 2026
- Affected product
- Philips Patient Information Centre iX (PIC iX) 4.x systems
- Category
- Medical device recalls
- Hazard
- 27/08/2026 Philips Patient Information Centre iX (PIC iX) 4.x systems Medical Device Product Correction Class II Hospital
Check affected Philips Patient Information Centre iX (PIC iX) 4.x systems 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 →Therapeutic Goods Administration · August 27, 2026
- Affected product
- VITROS Immunodiagnostic Products Anti-HAV Total Reagent Pack and
- Category
- Medical device recalls
- Hazard
- 27/08/2026 VITROS Immunodiagnostic Products Anti-HAV Total Reagent Pack and Total Calibrator. An in vitro diagnostic medical device (IVD) Medical Device Product Correction Class II Hospital
Check affected VITROS Immunodiagnostic Products Anti-HAV Total Reagent Pack and identifiers →Therapeutic Goods Administration · August 27, 2026
- Affected product
- Battery Pack SP with WiFi
- Category
- Medical device recalls, Consumer product recalls
- Hazard
- 27/08/2026 Battery Pack SP with WiFi Medical Device Recall Class III Hospital
Check affected Battery Pack SP with WiFi 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 26, 2026
- Affected product
- MEDUMAT Standard2 ventilators
- Category
- Medical device recalls
- Hazard
- 26/08/2026 MEDUMAT Standard2 ventilators Medical Device Product Correction Class II Hospital
Check affected MEDUMAT Standard2 ventilators identifiers →Therapeutic Goods Administration · August 26, 2026
- Affected product
- ForeSight Oximeter Cable
- Category
- Medical device recalls
- Hazard
- 26/08/2026 ForeSight Oximeter Cable Medical Device Product Correction Class II Hospital
Check affected ForeSight Oximeter Cable identifiers →Therapeutic Goods Administration · August 24, 2026
- Affected product
- Neoss Guide Implant Inserters
- Category
- Medical device recalls
- Hazard
- 24/08/2026 Neoss Guide Implant Inserters Medical Device Recall Class III Hospital
Check affected Neoss Guide Implant Inserters identifiers →Therapeutic Goods Administration · August 24, 2026
- Affected product
- Dexcom G7 iOS App
- Category
- Medical device recalls
- Hazard
- 24/08/2026 Dexcom G7 iOS App Medical Device Product Correction Class II Consumer
Check affected Dexcom G7 iOS App identifiers →Therapeutic Goods Administration · August 24, 2026
- Affected product
- Dexcom G7 App
- Category
- Medical device recalls
- Hazard
- 24/08/2026 Dexcom G7 App Medical Device Product Correction Class II Consumer
Check affected Dexcom G7 App identifiers →Therapeutic Goods Administration · August 24, 2026
- Affected product
- Fludeoxyglucose (18F) Injection (FDG)
- Category
- Medical device recalls
- Hazard
- 24/08/2026 Fludeoxyglucose (18F) Injection (FDG) Medicine Product Alert Class II Hospital
Check affected Fludeoxyglucose (18F) Injection (FDG) identifiers →Therapeutic Goods Administration · August 24, 2026
- Affected product
- Carescape Central Station (CSCS) V3.0.x
- Category
- Medical device recalls
- Hazard
- 24/08/2026 Carescape Central Station (CSCS) V3.0.x Medical Device Product Correction Class II Hospital
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
- 21/08/2026 All GEM PAKs for GEM Premier 5000 with iQM2 and GEM Premier 7000 with iQM3. An in vitro diagnostic medical device (IVD). Medical Device Product Correction Class II Hospital
Check affected All GEM PAKs for GEM Premier 5000 with iQM2 and GEM Premier 7000 identifiers →Therapeutic Goods Administration · August 21, 2026
- Affected product
- Imager II Angiographic Catheters
- Category
- Medical device recalls
- Hazard
- 21/08/2026 Imager II Angiographic Catheters Medical Device Recall Class II Hospital
Check affected Imager II Angiographic Catheters identifiers →Therapeutic Goods Administration · August 21, 2026
- Affected product
- Tooth Mousse Plus - Strawberry Flavour
- Category
- Medical device recalls
- Hazard
- 21/08/2026 Tooth Mousse Plus - Strawberry Flavour Medical Device Recall Class III Retail
Check affected Tooth Mousse Plus - Strawberry Flavour identifiers →Therapeutic Goods Administration · August 21, 2026
- Affected product
- Percussionaire IPV Systems
- Category
- Medical device recalls
- Hazard
- 21/08/2026 Percussionaire IPV Systems Medical Device Product Correction Class I Hospital
Check affected Percussionaire IPV Systems identifiers →Therapeutic Goods Administration · August 21, 2026
- Affected product
- Automated Impella Controller (AIC)
- Category
- Medical device recalls
- Hazard
- 21/08/2026 Automated Impella Controller (AIC) Medical Device Product Correction Class I Hospital
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 21, 2026
- Affected product
- BIOFIRE FILMARRAY TORCH System Base. An in vitro diagnostic medical
- Category
- Medical device recalls
- Hazard
- 21/08/2026 BIOFIRE FILMARRAY TORCH System Base. An in vitro diagnostic medical device (IVD). Medical Device Product Correction Class II Hospital
Check affected BIOFIRE FILMARRAY TORCH System Base. An in vitro diagnostic medical identifiers →Therapeutic Goods Administration · August 21, 2026
- Affected product
- VELA Tango 700E Mobility Chair
- Category
- Medical device recalls
- Hazard
- 21/08/2026 VELA Tango 700E Mobility Chair Medical Device Product Correction Class II Consumer
Check affected VELA Tango 700E Mobility Chair identifiers →Therapeutic Goods Administration · August 20, 2026
- Affected product
- Renuvion APR Handpiece
- Category
- Medical device recalls
- Hazard
- 20/08/2026 Renuvion APR Handpiece Medical Device Product Correction Class III Hospital
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
- 20/08/2026 Clearview, Innovacon, InstAlert and Surestep hCG Tests. An in vitro diagnostic medical device (IVD). Medical Device Product Correction Class II Hospital
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
- MicroVue SC5b-9 Plus EIA. An in vitro diagnostic medical device
- Category
- Medical device recalls
- Hazard
- 19/08/2026 MicroVue SC5b-9 Plus EIA. An in vitro diagnostic medical device (IVD) Medical Device Recall Class II Hospital
Check affected MicroVue SC5b-9 Plus EIA. An in vitro diagnostic medical device identifiers →Therapeutic Goods Administration · August 19, 2026
- Affected product
- Movicol Lemon & Lime 30s, Movicol Chocolate 30s, Movicol Junior
- Category
- Medical device recalls
- Hazard
- 19/08/2026 Movicol Lemon & Lime 30s, Movicol Chocolate 30s, Movicol Junior Flavour Free 30s Medicine Recall Class III Retail
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
- 19/08/2026 S7XTRA 200 Tub Wipes Medical Device Recall Class III Retail
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
- Any consumers who have a peanut allergy or intolerance may have a reaction if the product is consumed.
Check affected Chen Foods - Mr Chen's Szechuan Chilli Oil - 250g identifiers →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 →
