Therapeutic Goods Administration · September 16, 2026
- Affected product
- InterStim SureScan MRI Leads & InterStim Percutaneous Extension
- Category
- Medical device recalls
- Hazard
- 16/09/2026 InterStim SureScan MRI Leads & InterStim Percutaneous Extension Medical Device Product Alert Class II Hospital
Check affected InterStim SureScan MRI Leads & InterStim Percutaneous Extension identifiers →Therapeutic Goods Administration · September 16, 2026
- Affected product
- Tube Micro SST. An in vitro diagnostic medical device (IVD)
- Category
- Medical device recalls
- Hazard
- 16/09/2026 Tube Micro SST. An in vitro diagnostic medical device (IVD). Medical Device Recall Class II Hospital
Check affected Tube Micro SST. An in vitro diagnostic medical device (IVD) identifiers →Therapeutic Goods Administration · September 16, 2026
- Affected product
- Steriking Paper-Laminate Pouches
- Category
- Medical device recalls
- Hazard
- 16/09/2026 Steriking Paper-Laminate Pouches Medical Device Product Correction Class III Hospital
Check affected Steriking Paper-Laminate Pouches identifiers →Therapeutic Goods Administration · September 16, 2026
- Affected product
- N Rheumatology Standard SL. An in vitro diagnostic medical device
- Category
- Medical device recalls
- Hazard
- 16/09/2026 N Rheumatology Standard SL. An in vitro diagnostic medical device (IVD). Medical Device Product Correction Class III Hospital
Check affected N Rheumatology Standard SL. An in vitro diagnostic medical device identifiers →Therapeutic Goods Administration · September 15, 2026
- Affected product
- Dako Slide Racks - 10 pieces CoverStainer. An in vitro diagnostic
- Category
- Medical device recalls
- Hazard
- 15/09/2026 Dako Slide Racks - 10 pieces CoverStainer. An in vitro diagnostic medical device (IVD). Medical Device Product Correction Class III Hospital
Check affected Dako Slide Racks - 10 pieces CoverStainer. An in vitro diagnostic identifiers →ACCC Product Safety Australia · September 15, 2026
- Affected product
- Qinbeer silicone pull string toys sold through Amazon
- 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 Qinbeer silicone pull string toys sold through Amazon identifiers →Therapeutic Goods Administration · September 15, 2026
- Affected product
- GORE CARDIOFORM Septal Occluder (GSO)
- Category
- Medical device recalls
- Hazard
- 15/09/2026 GORE CARDIOFORM Septal Occluder (GSO) Medical Device Product Correction Class III Hospital
Check affected GORE CARDIOFORM Septal Occluder (GSO) identifiers →ACCC Product Safety Australia · September 15, 2026
- Affected product
- Rota Cota Trade Pro 3 Paint Spray Gun
- Category
- Consumer product recalls
- Hazard
- of unintentional discharge. The hazards to consumers Risk of serious eye injury and high-pressure skin injury if the safety lock unintentionally disengages and the spray gun discharges paint when the trigger is pressed. What consumers should do Immediately…
Check affected Rota Cota Trade Pro 3 Paint Spray Gun identifiers →ACCC Product Safety Australia · September 14, 2026
- Affected product
- Narva Ultima wiring harness for use with Ultima MK3 215 hybrid
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury or death and/or property damage from fire if the harness overheats and catches fire. Incidents have occurred, including a vehicle catching fire. What consumers should do Stop using
Check affected Narva Ultima wiring harness for use with Ultima MK3 215 hybrid identifiers →Therapeutic Goods Administration · September 14, 2026
- Affected product
- MR systems with SW versions R5 & R11
- Category
- Medical device recalls
- Hazard
- 14/09/2026 MR systems with SW versions R5 & R11 Medical Device Product Correction Class II Hospital
Check affected MR systems with SW versions R5 & R11 identifiers →Therapeutic Goods Administration · September 14, 2026
- Affected product
- Amplatzer Amulet Left Atrial Appendage Occluder
- Category
- Medical device recalls
- Hazard
- 14/09/2026 Amplatzer Amulet Left Atrial Appendage Occluder Medical Device Product Correction Class I Hospital
Check affected Amplatzer Amulet Left Atrial Appendage Occluder identifiers →Therapeutic Goods Administration · September 14, 2026
- Affected product
- BIOFIRE FILMARRAY Pneumonia Plus Panel, 6 Tests. An in vitro
- Category
- Medical device recalls
- Hazard
- 14/09/2026 BIOFIRE FILMARRAY Pneumonia Plus Panel, 6 Tests. An in vitro diagnostic medical device (IVD). Medical Device Product Alert Class II Hospital
Check affected BIOFIRE FILMARRAY Pneumonia Plus Panel, 6 Tests. An in vitro identifiers →Therapeutic Goods Administration · September 14, 2026
- Affected product
- SOLTIVE SuperPulsed laser fibre devices
- Category
- Medical device recalls
- Hazard
- 14/09/2026 SOLTIVE SuperPulsed laser fibre devices Medical Device Recall Class II Hospital
Check affected SOLTIVE SuperPulsed laser fibre devices identifiers →Food Standards Australia New Zealand · September 11, 2026
- Affected product
- Alog Australian Wholesalers Pty Ltd - Red Hat Cookia Matcha
- Category
- Food recalls
- Hazard
- Any consumers who have an egg, milk and/or soy allergy or intolerance may have a reaction if the product is consumed.
Check affected Alog Australian Wholesalers Pty Ltd - Red Hat Cookia Matcha identifiers →ACCC Product Safety Australia · September 11, 2026
- Affected product
- Coloured contact lenses designed for cosplay and makeup applications
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of irritation or serious eye infection that can impact users’ vision when exposed to these bacteria complex. An incident has occurred overseas. What consumers should do Stop using these
Check affected Coloured contact lenses designed for cosplay and makeup applications identifiers →ACCC Product Safety Australia · September 11, 2026
- Affected product
- Merino Essentials Pointelle Kimono Stretch & Grow and Merino
- Category
- Consumer product recalls
- Hazard
- The hazards to consumers Risk of serious injury or death from choking and asphyxiation if a fastener separates from a garment and a child places it in their mouth. Incidents of the fasteners detaching have occurred. What consumers should do Stop using these…
Check affected Merino Essentials Pointelle Kimono Stretch & Grow and Merino identifiers →Therapeutic Goods Administration · September 11, 2026
- Affected product
- LIFEPAK 35 Monitor/Defibrillator
- Category
- Medical device recalls
- Hazard
- 11/09/2026 LIFEPAK 35 Monitor/Defibrillator Medical Device Product Correction Class II Hospital
Check affected LIFEPAK 35 Monitor/Defibrillator identifiers →Food Standards Australia New Zealand · September 10, 2026
- Affected product
- JC Seafood Sweet Chilli & Lime Salmon Portions - 275g
- Category
- Food recalls
- Hazard
- Any consumers who have a soy allergy or intolerance may have a reaction if the product is consumed.
Check affected JC Seafood Sweet Chilli & Lime Salmon Portions - 275g identifiers →Food Standards Australia New Zealand · September 9, 2026
- Affected product
- Greenstorm Foods t/a Austral Herbs - Certified Organic Premium
- Category
- Food recalls
- Hazard
- Food products containing metal contaminants may cause illness/injury if consumed.
Check affected Greenstorm Foods t/a Austral Herbs - Certified Organic Premium identifiers →ACCC Product Safety Australia · September 9, 2026
- Affected product
- Gingham Flower hair accessory set
- Category
- Consumer product recalls
- Hazard
- The hazards to consumers Risk of serious injury or death from choking or asphyxiation if the centre button of the flower clip separates when pulled from the product and a child swallows it. What consumers should do Stop using the hair accessory immediately and…
Check affected Gingham Flower hair accessory set identifiers →Therapeutic Goods Administration · September 9, 2026
- Affected product
- DxC 500 AU Clinical Chemistry Analyser & DxC 500i Clinical Analyser
- Category
- Medical device recalls
- Hazard
- 9/09/2026 DxC 500 AU Clinical Chemistry Analyser & DxC 500i Clinical Analyser. An in vitro diagnostic medical device (IVD). Medical Device Product Correction Class II Hospital
Check affected DxC 500 AU Clinical Chemistry Analyser & DxC 500i Clinical Analyser identifiers →Therapeutic Goods Administration · September 8, 2026
- Affected product
- Aspire Active Air 8 Pressure Care Air Mattress
- Category
- Medical device recalls
- Hazard
- 8/09/2026 Aspire Active Air 8 Pressure Care Air Mattress Medical Device Product Alert Class II Consumer
Check affected Aspire Active Air 8 Pressure Care Air Mattress identifiers →ACCC Product Safety Australia · September 8, 2026
- Affected product
- Love to Dream Sleep Machine
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury, death and/or property damage from fire if the battery overheats and starts a fire. Incidents have occurred with 1 incident causing property damage. What consumers should do Stop using the
Check affected Love to Dream Sleep Machine identifiers →Therapeutic Goods Administration · September 8, 2026
- Affected product
- Various Vitaco Nutra-Life and Musashi Products
- Category
- Medical device recalls
- Hazard
- 8/09/2026 Various Vitaco Nutra-Life and Musashi Products Medicine Product Alert Class III Consumer
Check affected Various Vitaco Nutra-Life and Musashi Products identifiers →Therapeutic Goods Administration · September 7, 2026
- Affected product
- TCM Tosca and TCM CombiM
- Category
- Medical device recalls
- Hazard
- 7/09/2026 TCM Tosca and TCM CombiM Medical Device Product Correction Class II Hospital
Check affected TCM Tosca and TCM CombiM identifiers →Therapeutic Goods Administration · September 7, 2026
- Affected product
- Femoral Head (L) MC Allograft
- Category
- Medical device recalls
- Hazard
- 7/09/2026 Femoral Head (L) MC Allograft Biological Product Alert Class II Hospital
Check affected Femoral Head (L) MC Allograft identifiers →Therapeutic Goods Administration · September 7, 2026
- Affected product
- Carestation 850 and 850c Anesthesia Systems
- Category
- Medical device recalls
- Hazard
- 7/09/2026 Carestation 850 and 850c Anesthesia Systems Medical Device Product Correction Class II Hospital
Check affected Carestation 850 and 850c Anesthesia Systems identifiers →Therapeutic Goods Administration · September 7, 2026
- Affected product
- Philips CT Rembra systems
- Category
- Medical device recalls
- Hazard
- 7/09/2026 Philips CT Rembra systems Medical Device Product Correction Class II Hospital
Check affected Philips CT Rembra systems identifiers →ACCC Product Safety Australia · September 7, 2026
- Affected product
- Adora Pecker Finger vibrator
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious burn injuries, death or property damage if the cable overheats or catches fire while connected to any USB power source. Incidents of overheating have occurred. What consumers should do Stop using the product immediately and unplug…
Check affected Adora Pecker Finger vibrator identifiers →Food Standards Australia New Zealand · September 4, 2026
- Affected product
- Bottega 1995 - Brie Mon Sire - 1Kg
- Category
- Food recalls
- Hazard
- Listeria monocytogenes may cause severe illness in pregnant women, unborn babies, neonates, the elderly, and immunocompromised individuals. The general population can also become ill from consuming food contaminated with Listeria monocytogenes .
Check affected Bottega 1995 - Brie Mon Sire - 1Kg identifiers →Therapeutic Goods Administration · September 4, 2026
- Affected product
- VentStar Resus Neo and VentStar Resuscitaire
- Category
- Medical device recalls
- Hazard
- 4/09/2026 VentStar Resus Neo and VentStar Resuscitaire Medical Device Product Correction Class I Hospital
Check affected VentStar Resus Neo and VentStar Resuscitaire identifiers →Therapeutic Goods Administration · September 4, 2026
- Affected product
- Femoral Head (R) Allograft
- Category
- Medical device recalls
- Hazard
- 4/09/2026 Femoral Head (R) Allograft Biological Product Alert Class II Hospital
Check affected Femoral Head (R) Allograft identifiers →ACCC Product Safety Australia · September 4, 2026
- Affected product
- Farm to Table Play Kitchen
- Category
- Consumer product recalls
- Hazard
- Children’s clothing can become snagged on these hooks, posing a strangulation hazard. The hazards to consumers Risk of serious injury or death from strangulation and asphyxiation if a child is snagged on an accessory hook. An incident has occurred in the USA…
Check affected Farm to Table Play Kitchen identifiers →Therapeutic Goods Administration · September 4, 2026
- Affected product
- HeartHero Elliot Automated External Defibrillator (AED)
- Category
- Medical device recalls
- Hazard
- 4/09/2026 HeartHero Elliot Automated External Defibrillator (AED) Medical Device Product Correction Class I Consumer
Check affected HeartHero Elliot Automated External Defibrillator (AED) identifiers →Therapeutic Goods Administration · September 3, 2026
- Affected product
- IntelePACS – InteleConnect Portal / Tech Portal Version
- Category
- Medical device recalls
- Hazard
- 3/09/2026 IntelePACS – InteleConnect Portal / Tech Portal Version Medical Device Product Correction Class I Hospital
Check affected IntelePACS – InteleConnect Portal / Tech Portal Version identifiers →Therapeutic Goods Administration · September 3, 2026
- Affected product
- NDI Passive Spheres and Medtronic Biopsy Needle Kit
- Category
- Medical device recalls
- Hazard
- 3/09/2026 NDI Passive Spheres and Medtronic Biopsy Needle Kit Medical Device Recall Class II Hospital
Check affected NDI Passive Spheres and Medtronic Biopsy Needle Kit identifiers →Therapeutic Goods Administration · September 3, 2026
- Affected product
- Deep Heat Extra Strength 100g Cream
- Category
- Medical device recalls
- Hazard
- 3/09/2026 Deep Heat Extra Strength 100g Cream Medicine Recall Class II Consumer
Check affected Deep Heat Extra Strength 100g Cream identifiers →Therapeutic Goods Administration · September 3, 2026
- Affected product
- LEO+ Self-Expanding Nitinol Stent (Stent, vascular, intracranial)
- Category
- Medical device recalls
- Hazard
- 3/09/2026 LEO+ Self-Expanding Nitinol Stent (Stent, vascular, intracranial) and Eclipse Balloon Catheter (Catheter, intravascular, occluding) Medical Device Recall Class II Hospital
Check affected LEO+ Self-Expanding Nitinol Stent (Stent, vascular, intracranial) identifiers →Therapeutic Goods Administration · September 2, 2026
- Affected product
- MITOMYCIN OMEGAPHARM mitomycin powder for injection 20mg vial
- Category
- Medical device recalls
- Hazard
- 2/09/2026 MITOMYCIN OMEGAPHARM mitomycin powder for injection 20mg vial Medicine Product Alert Class II Hospital
Check affected MITOMYCIN OMEGAPHARM mitomycin powder for injection 20mg vial identifiers →ACCC Product Safety Australia · September 2, 2026
- Affected product
- XL magnetic building blocks
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury or death from choking and asphyxiation if a child places small parts inside their mouth. There is also a risk of serious injury from laceration from sharp points. Incidents have occurred. What consumers should do Stop using…
Check affected XL magnetic building blocks identifiers →
