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 →Food Standards Australia New Zealand · September 26, 2026
- Affected product
- Supercol Australia - Supercol Food and Liquid Thickener - 325g, 900g
- Category
- Food recalls
- Hazard
- Food products contaminated with cronobacter may cause illness if consumed.
Check affected Supercol Australia - Supercol Food and Liquid Thickener - 325g, 900g identifiers →Therapeutic Goods Administration · September 25, 2026
- Affected product
- Cefazolin 6,000mg in 0.9% Sodium Chloride in Surefuser + (10mL/hr)
- Category
- Medical device recalls
- Hazard
- 25/09/2026 Cefazolin 6,000mg in 0.9% Sodium Chloride in Surefuser + (10mL/hr) for Intravenous Infusion Medicine Recall Class II Hospital
Check affected Cefazolin 6,000mg in 0.9% Sodium Chloride in Surefuser + (10mL/hr) identifiers →ACCC Product Safety Australia · September 25, 2026
- Affected product
- Heeve® 3-Tonne 3.2m x 390mm Aluminium Loading Ramps
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of death or serious injury and/or property damage if the ramp collapses and causes heavy equipment to topple or fall. Incidents of the ramp failing have occurred. What consumers should do Stop using the affected ramps immediately. Affected…
Check affected Heeve® 3-Tonne 3.2m x 390mm Aluminium Loading Ramps identifiers →Therapeutic Goods Administration · September 25, 2026
- Affected product
- Philips Spectral CT with software version V5.0, V5.2, or V5.4
- Category
- Medical device recalls
- Hazard
- 25/09/2026 Philips Spectral CT with software version V5.0, V5.2, or V5.4 Medical Device Product Correction Class II Hospital
Check affected Philips Spectral CT with software version V5.0, V5.2, or V5.4 identifiers →ACCC Product Safety Australia · September 25, 2026
- Affected product
- S1 Dry Flush Sealing Toilet and S1 Adapter Kit
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury, death, and/or property damage if damaged batteries overheat, release smoke and toxic gas or catch fire. What consumers should do If the battery has been charged at temperatures under 3°C or if you are unsure: immediately…
Check affected S1 Dry Flush Sealing Toilet and S1 Adapter Kit identifiers →Therapeutic Goods Administration · September 25, 2026
- Affected product
- CareLink SmartSync Device Manager
- Category
- Medical device recalls
- Hazard
- 25/09/2026 CareLink SmartSync Device Manager Medical Device Product Correction Class II Hospital
Check affected CareLink SmartSync Device Manager identifiers →Therapeutic Goods Administration · September 25, 2026
- Affected product
- Carboplatin 270mg in 5% Glucose in polyolefin bag (freeflex) for
- Category
- Medical device recalls
- Hazard
- 25/09/2026 Carboplatin 270mg in 5% Glucose in polyolefin bag (freeflex) for intravenous infusion Medicine Recall Class II Hospital
Check affected Carboplatin 270mg in 5% Glucose in polyolefin bag (freeflex) for identifiers →Therapeutic Goods Administration · September 25, 2026
- Affected product
- Ventilation (tympanostomy) Tube 5PK Button 1.27 FLPL
- Category
- Medical device recalls
- Hazard
- 25/09/2026 Ventilation (tympanostomy) Tube 5PK Button 1.27 FLPL Medical Device Recall Class II Hospital
Check affected Ventilation (tympanostomy) Tube 5PK Button 1.27 FLPL identifiers →Therapeutic Goods Administration · September 24, 2026
- Affected product
- CareLink SmartSync Device Manager
- Category
- Medical device recalls
- Hazard
- 24/09/2026 CareLink SmartSync Device Manager Medical Device Product Correction Class II Hospital
Check affected CareLink SmartSync Device Manager identifiers →Therapeutic Goods Administration · September 24, 2026
- Affected product
- cobas c 303 analytical unit. An in vitro diagnostic medical device
- Category
- Medical device recalls
- Hazard
- 24/09/2026 cobas c 303 analytical unit. An in vitro diagnostic medical device (IVD) Medical Device Product Correction Class II Hospital
Check affected cobas c 303 analytical unit. An in vitro diagnostic medical device identifiers →Therapeutic Goods Administration · September 24, 2026
- Affected product
- SW-40 and SW-41 Rotors in Optima. An in vitro diagnostic medical
- Category
- Medical device recalls
- Hazard
- 24/09/2026 SW-40 and SW-41 Rotors in Optima. An in vitro diagnostic medical device (IVD). Medical Device Recall Class II Hospital
Check affected SW-40 and SW-41 Rotors in Optima. An in vitro diagnostic medical identifiers →Therapeutic Goods Administration · September 24, 2026
- Affected product
- Philips BV Pulsera and Zenition Systems
- Category
- Medical device recalls
- Hazard
- 24/09/2026 Philips BV Pulsera and Zenition Systems Medical Device Product Correction Class I Hospital
Check affected Philips BV Pulsera and Zenition Systems identifiers →Therapeutic Goods Administration · September 23, 2026
- Affected product
- Aisys CS2, Aisys CS2 with Et Control and S/5 Aisys Anesthesia
- Category
- Medical device recalls
- Hazard
- 23/09/2026 Aisys CS2, Aisys CS2 with Et Control and S/5 Aisys Anesthesia Systems Medical Device Product Correction Class II Hospital
Check affected Aisys CS2, Aisys CS2 with Et Control and S/5 Aisys Anesthesia identifiers →Therapeutic Goods Administration · September 23, 2026
- Affected product
- BD Alaris Point of Care Unit (PCU) Wireless ONLY
- Category
- Medical device recalls
- Hazard
- 23/09/2026 BD Alaris Point of Care Unit (PCU) Wireless ONLY Medical Device Product Correction Class II Hospital
Check affected BD Alaris Point of Care Unit (PCU) Wireless ONLY identifiers →Therapeutic Goods Administration · September 23, 2026
- Affected product
- Simplexa COVID-19 / Flu A/B & RSV Direct (MOL4450). An in vitro
- Category
- Medical device recalls
- Hazard
- 23/09/2026 Simplexa COVID-19 / Flu A/B & RSV Direct (MOL4450). An in vitro diagnostic medical device (IVD). Medical Device Recall Class III Hospital
Check affected Simplexa COVID-19 / Flu A/B & RSV Direct (MOL4450). An in vitro identifiers →Therapeutic Goods Administration · September 23, 2026
- Affected product
- Ethilon Nylon Suture BLK 45CM 6-0 S/A P-1 PRM
- Category
- Medical device recalls
- Hazard
- 23/09/2026 Ethilon Nylon Suture BLK 45CM 6-0 S/A P-1 PRM Medical Device Recall Class II Hospital
Check affected Ethilon Nylon Suture BLK 45CM 6-0 S/A P-1 PRM identifiers →Therapeutic Goods Administration · September 23, 2026
- Affected product
- Single Use Ligating Device Polyloop
- Category
- Medical device recalls
- Hazard
- 23/09/2026 Single Use Ligating Device Polyloop Medical Device Recall Class II Hospital
Check affected Single Use Ligating Device Polyloop identifiers →Therapeutic Goods Administration · September 22, 2026
- Affected product
- ID-DiaCell I-II-III. An in vitro diagnostic medical device (IVD)
- Category
- Medical device recalls
- Hazard
- 22/09/2026 ID-DiaCell I-II-III. An in vitro diagnostic medical device (IVD). Medical Device Recall Class II Hospital
Check affected ID-DiaCell I-II-III. An in vitro diagnostic medical device (IVD) identifiers →Therapeutic Goods Administration · September 21, 2026
- Affected product
- Certain Philips MR Systems with Diffusion Tensor Imaging (DTI)
- Category
- Medical device recalls
- Hazard
- 21/09/2026 Certain Philips MR Systems with Diffusion Tensor Imaging (DTI) Medical Device Product Correction Class II Hospital
Check affected Certain Philips MR Systems with Diffusion Tensor Imaging (DTI) identifiers →Therapeutic Goods Administration · September 21, 2026
- Affected product
- LABScreen Mixed Class I & II. An in vitro diagnostic medical device
- Category
- Medical device recalls
- Hazard
- 21/09/2026 LABScreen Mixed Class I & II. An in vitro diagnostic medical device (IVD). Medical Device Product Correction Class III Hospital
Check affected LABScreen Mixed Class I & II. An in vitro diagnostic medical device identifiers →Therapeutic Goods Administration · September 21, 2026
- Affected product
- Allcare Ultrasound Gel 5L
- Category
- Medical device recalls
- Hazard
- 21/09/2026 Allcare Ultrasound Gel 5L Medical Device Recall Class II Hospital
Check affected Allcare Ultrasound Gel 5L identifiers →Therapeutic Goods Administration · September 21, 2026
- Affected product
- Cisplatin 57.6mg in 0.9% Sodium Chloride in Polyolefin Bag
- Category
- Medical device recalls
- Hazard
- 21/09/2026 Cisplatin 57.6mg in 0.9% Sodium Chloride in Polyolefin Bag (Freeflex) for Intravenous Infusion & Cisplatin 75mg in 0.9% Sodium Chloride in Polyolefin Bag (Freeflex) for Intravenous Infusion Medicine Recall Class II Hospital
Check affected Cisplatin 57.6mg in 0.9% Sodium Chloride in Polyolefin Bag identifiers →ACCC Product Safety Australia · September 21, 2026
- Affected product
- Fidlock HERMETIC Medi size Dry Bag
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious internal injuries or death if a child swallows more than one high-powered magnet as they stick together in the child’s intestine or other digestive tissue. Risk of serious injury or death from choking. What consumers should do…
Check affected Fidlock HERMETIC Medi size Dry Bag identifiers →Therapeutic Goods Administration · September 21, 2026
- Affected product
- Diaguru Ultrasound Gel Blue 250mL
- Category
- Medical device recalls
- Hazard
- 21/09/2026 Diaguru Ultrasound Gel Blue 250mL Medical Device Recall Class II Hospital
Check affected Diaguru Ultrasound Gel Blue 250mL identifiers →Therapeutic Goods Administration · September 21, 2026
- Affected product
- LithoVue Elite StoneSmart Connect Console Power Adaptor
- Category
- Medical device recalls
- Hazard
- 21/09/2026 LithoVue Elite StoneSmart Connect Console Power Adaptor Medical Device Product Correction Class III Hospital
Check affected LithoVue Elite StoneSmart Connect Console Power Adaptor identifiers →Therapeutic Goods Administration · September 18, 2026
- Affected product
- CLARITY Blue Ultrasound Gel Water soluble & hypoallergenic Bottle
- Category
- Medical device recalls
- Hazard
- 18/09/2026 CLARITY Blue Ultrasound Gel Water soluble & hypoallergenic Bottle 250mL Medical Device Recall Class II Hospital
Check affected CLARITY Blue Ultrasound Gel Water soluble & hypoallergenic Bottle identifiers →ACCC Product Safety Australia · September 18, 2026
- Affected product
- Mise en scéne Hello Bubble Foam Hair Colour
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury from a reaction to the contents in the product if consumers are unable to identify and read the warning label before use. What consumers should do Consumers should immediately stop using the product. Consumers can return the…
Check affected Mise en scéne Hello Bubble Foam Hair Colour identifiers →Therapeutic Goods Administration · September 18, 2026
- Affected product
- FLEBOGAMMA 10%DIF normal immunoglobulin (Human) 20g/200ml
- Category
- Medical device recalls
- Hazard
- 18/09/2026 FLEBOGAMMA 10%DIF normal immunoglobulin (Human) 20g/200ml intravenous use injection vial Medicine Recall Class II Hospital
Check affected FLEBOGAMMA 10%DIF normal immunoglobulin (Human) 20g/200ml identifiers →ACCC Product Safety Australia · September 18, 2026
- Affected product
- Baby Sensory Activity 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 toys and the child places them in their mouth. What consumers should do Stop using the…
Check affected Baby Sensory Activity Toys identifiers →ACCC Product Safety Australia · September 18, 2026
- Affected product
- Salon de Pro unscented hair colour fast dye cream
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury from a reaction to the contents in the product if consumers are unable to identify and read the warning label before use. What consumers should do Consumers should immediately stop using the product. Consumers can return the…
Check affected Salon de Pro unscented hair colour fast dye cream identifiers →ACCC Product Safety Australia · September 18, 2026
- Affected product
- AK Flower Bouquet Toy
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- to consumers Risk of serious injury to face or eyes of young children during play or use if the metal rod is exposed from the toy. What consumers should do Stop using the toy immediately and place out of reach of any children. Return the toy to an Adairs…
Check affected AK Flower Bouquet Toy identifiers →ACCC Product Safety Australia · September 18, 2026
- Affected product
- 4-key keyboard switch clicker key chain
- 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. An incident of battery ingestion has occurred. Serious injury can occur in as little as 2 hours and the…
Check affected 4-key keyboard switch clicker key chain identifiers →Therapeutic Goods Administration · September 18, 2026
- Affected product
- Safsite Valve VV/O Extra Cap RV1000NC
- Category
- Medical device recalls
- Hazard
- 18/09/2026 Safsite Valve VV/O Extra Cap RV1000NC Medical Device Recall Class II Hospital
Check affected Safsite Valve VV/O Extra Cap RV1000NC identifiers →Therapeutic Goods Administration · September 18, 2026
- Affected product
- Philips Spectral CT Systems
- Category
- Medical device recalls
- Hazard
- 18/09/2026 Philips Spectral CT Systems Medical Device Product Correction Class II Hospital
Check affected Philips Spectral CT Systems identifiers →ACCC Product Safety Australia · September 18, 2026
- Affected product
- Kao Liese Prettia Bubble Hair Colour
- Category
- Consumer product recalls
- Hazard
- to consumers Risk of serious injury from a reaction to the contents in the product if consumers are unable to identify and read the warning label before use. What consumers should do Consumers should immediately stop using the product. Consumers can return the…
Check affected Kao Liese Prettia Bubble Hair Colour identifiers →ACCC Product Safety Australia · September 17, 2026
- Affected product
- The Wonderland Collection K Mini Baby Thermal Drink Bottles
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- to consumers Risk of serious injury or death from choking if small parts detach from the bottle and a child places them in their mouth. What consumers should do Stop using the product immediately and keep out of reach of children. Return the product to your…
Check affected The Wonderland Collection K Mini Baby Thermal Drink Bottles identifiers →Therapeutic Goods Administration · September 17, 2026
- Affected product
- Direxion and Direxion HIFLO Microcatheters
- Category
- Medical device recalls
- Hazard
- 17/09/2026 Direxion and Direxion HIFLO Microcatheters Medical Device Recall Class II Hospital
Check affected Direxion and Direxion HIFLO Microcatheters identifiers →Therapeutic Goods Administration · September 17, 2026
- Affected product
- OmniaSecure MRI SureScan Defibrillation Leads
- Category
- Medical device recalls
- Hazard
- 17/09/2026 OmniaSecure MRI SureScan Defibrillation Leads Medical Device Recall Class II Hospital
Check affected OmniaSecure MRI SureScan Defibrillation Leads identifiers →Therapeutic Goods Administration · September 17, 2026
- Affected product
- Newport HT70, Newport HT70 Plus Ventilators and PCBA Service Parts
- Category
- Medical device recalls
- Hazard
- 17/09/2026 Newport HT70, Newport HT70 Plus Ventilators and PCBA Service Parts Medical Device Recall Class I Hospital
Check affected Newport HT70, Newport HT70 Plus Ventilators and PCBA Service Parts identifiers →
