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 →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 →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 →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 →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 →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 →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 →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 →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 →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 →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 →
