Therapeutic Goods Administration · October 9, 2026
- Affected product
- AYUNA AMA CARE 60 /100 VEG capsules
- Category
- Medical device recalls
- Hazard
- 9/10/2026 AYUNA AMA CARE 60 /100 VEG capsules Medicine Recall Class I Consumer
Check affected AYUNA AMA CARE 60 /100 VEG capsules identifiers →Therapeutic Goods Administration · October 9, 2026
- Affected product
- TraumaFix Professional Pelvic Splint
- Category
- Medical device recalls
- Hazard
- 9/10/2026 TraumaFix Professional Pelvic Splint Medical Device Recall Class II Hospital
Check affected TraumaFix Professional Pelvic Splint identifiers →Therapeutic Goods Administration · October 9, 2026
- Affected product
- PORTABLE X-RAY UNIT FDR XAIR
- Category
- Medical device recalls
- Hazard
- 9/10/2026 PORTABLE X-RAY UNIT FDR XAIR Medical Device Product Correction Class III Hospital
Check affected PORTABLE X-RAY UNIT FDR XAIR identifiers →Therapeutic Goods Administration · October 9, 2026
- Affected product
- Atellica CH HDL Cholesterol (HDLC) & Atellica CH Total Protein_2
- Category
- Medical device recalls
- Hazard
- 9/10/2026 Atellica CH HDL Cholesterol (HDLC) & Atellica CH Total Protein_2 (TP_2). An in vitro diagnostic medical device (IVD). Medical Device Product Correction Class II Hospital
Check affected Atellica CH HDL Cholesterol (HDLC) & Atellica CH Total Protein_2 identifiers →Therapeutic Goods Administration · October 9, 2026
- Affected product
- LULA Nicotine Salt Pods - Unflavoured 50 mg/mL
- Category
- Medical device recalls
- Hazard
- 9/10/2026 LULA Nicotine Salt Pods - Unflavoured 50 mg/mL Medical Device Recall Class II Retail
Check affected LULA Nicotine Salt Pods - Unflavoured 50 mg/mL identifiers →Therapeutic Goods Administration · October 8, 2026
- Affected product
- Troponin T Control. An in vitro diagnostic medical device (IVD)
- Category
- Medical device recalls
- Hazard
- 8/10/2026 Troponin T Control. An in vitro diagnostic medical device (IVD). Medical Device Recall Class II Hospital
Check affected Troponin T Control. An in vitro diagnostic medical device (IVD) identifiers →Therapeutic Goods Administration · October 8, 2026
- Affected product
- Faulding Immune Combat 100s
- Category
- Medical device recalls
- Hazard
- 8/10/2026 Faulding Immune Combat 100s Medicine Recall Class I Consumer
Check affected Faulding Immune Combat 100s identifiers →Therapeutic Goods Administration · October 8, 2026
- Affected product
- Gemcitabine 1,425mg in 0.9% Sodium Chloride in Polyolefin Bag
- Category
- Medical device recalls
- Hazard
- 8/10/2026 Gemcitabine 1,425mg in 0.9% Sodium Chloride in Polyolefin Bag (Freeflex) for Intravenous Infusion Medicine Recall Class II Hospital
Check affected Gemcitabine 1,425mg in 0.9% Sodium Chloride in Polyolefin Bag identifiers →Therapeutic Goods Administration · October 8, 2026
- Affected product
- BioCeuticals ArmaForce 30, 60 & 120 tablets and BioCeuticals
- Category
- Medical device recalls
- Hazard
- 8/10/2026 BioCeuticals ArmaForce 30, 60 & 120 tablets and BioCeuticals Clinical ImmuneForce 60 tablets Medicine Recall Class I Consumer
Check affected BioCeuticals ArmaForce 30, 60 & 120 tablets and BioCeuticals identifiers →Therapeutic Goods Administration · October 7, 2026
- Affected product
- Femoral Head (L) Non-irradiated, Non-processed
- Category
- Medical device recalls
- Hazard
- 7/10/2026 Femoral Head (L) Non-irradiated, Non-processed Biological Product Alert Class II Hospital
Check affected Femoral Head (L) Non-irradiated, Non-processed identifiers →Therapeutic Goods Administration · October 6, 2026
- Affected product
- Philips Radiography 7000 M system
- Category
- Medical device recalls
- Hazard
- 6/10/2026 Philips Radiography 7000 M system Medical Device Product Correction Class II Hospital
Check affected Philips Radiography 7000 M system identifiers →Therapeutic Goods Administration · October 6, 2026
- Affected product
- Immune Support Echinacea Plus, 60 Film Coated Tablets
- Category
- Medical device recalls
- Hazard
- 6/10/2026 Immune Support Echinacea Plus, 60 Film Coated Tablets Medicine Recall Class I Consumer
Check affected Immune Support Echinacea Plus, 60 Film Coated Tablets identifiers →Therapeutic Goods Administration · October 6, 2026
- Affected product
- Li-Ion Rechargeable Battery for corpuls CPR
- Category
- Medical device recalls, Consumer product recalls
- Hazard
- 6/10/2026 Li-Ion Rechargeable Battery for corpuls CPR Medical Device Recall Class I Hospital
Check affected Li-Ion Rechargeable Battery for corpuls CPR identifiers →Therapeutic Goods Administration · October 6, 2026
- Affected product
- Philips MR Systems on R11, R12.1.1, and R12.2.0
- Category
- Medical device recalls
- Hazard
- 6/10/2026 Philips MR Systems on R11, R12.1.1, and R12.2.0 Medical Device Product Correction Class III Hospital
Check affected Philips MR Systems on R11, R12.1.1, and R12.2.0 identifiers →Therapeutic Goods Administration · October 6, 2026
- Affected product
- PM Lung Support II
- Category
- Medical device recalls
- Hazard
- 6/10/2026 PM Lung Support II Medicine Recall Class I Consumer
Check affected PM Lung Support II identifiers →Therapeutic Goods Administration · October 2, 2026
- Affected product
- VERSA Accessory Cart
- Category
- Medical device recalls
- Hazard
- 2/10/2026 VERSA Accessory Cart Medical Device Product Correction Class II Hospital
Check affected VERSA Accessory Cart identifiers →Therapeutic Goods Administration · October 2, 2026
- Affected product
- HAMILTON-C6 Ventilator
- Category
- Medical device recalls
- Hazard
- 2/10/2026 HAMILTON-C6 Ventilator Medical Device Product Correction Class II Hospital
Check affected HAMILTON-C6 Ventilator identifiers →Therapeutic Goods Administration · October 2, 2026
- Affected product
- FLUMAZENIL-BAXTER flumazenil 0.5 mg/5 mL solution for injection
- Category
- Medical device recalls
- Hazard
- 2/10/2026 FLUMAZENIL-BAXTER flumazenil 0.5 mg/5 mL solution for injection ampoule Medicine Recall Class II Hospital
Check affected FLUMAZENIL-BAXTER flumazenil 0.5 mg/5 mL solution for injection identifiers →Therapeutic Goods Administration · October 2, 2026
- Affected product
- Sharp Uterine Curettes / Gynaecological Curettes
- Category
- Medical device recalls
- Hazard
- 2/10/2026 Sharp Uterine Curettes / Gynaecological Curettes Medical Device Product Correction Class II Hospital
Check affected Sharp Uterine Curettes / Gynaecological Curettes identifiers →Therapeutic Goods Administration · October 1, 2026
- Affected product
- CHEMISTS' OWN PROVANCE Immune Defence & 28 PLUS Immune Defence
- Category
- Medical device recalls
- Hazard
- 1/10/2026 CHEMISTS' OWN PROVANCE Immune Defence & 28 PLUS Immune Defence Medicine Recall Class I Consumer
Check affected CHEMISTS' OWN PROVANCE Immune Defence & 28 PLUS Immune Defence identifiers →Therapeutic Goods Administration · October 1, 2026
- Affected product
- KayserBetten Safe Surround Genie Bed
- Category
- Medical device recalls
- Hazard
- 1/10/2026 KayserBetten Safe Surround Genie Bed Medical Device Product Correction Class I Consumer
Check affected KayserBetten Safe Surround Genie Bed identifiers →Therapeutic Goods Administration · October 1, 2026
- Affected product
- ADRENALINE-LINK 1:10,000 1mg/10ml ADRENALINE (EPINEPHRINE) ACID
- Category
- Medical device recalls
- Hazard
- 1/10/2026 ADRENALINE-LINK 1:10,000 1mg/10ml ADRENALINE (EPINEPHRINE) ACID TARTRATE INJECTION 1MG IN 10ML BP PRE-FILLED SYRINGE (PFS) Medicine Product Correction Class II Hospital
Check affected ADRENALINE-LINK 1:10,000 1mg/10ml ADRENALINE (EPINEPHRINE) ACID identifiers →Therapeutic Goods Administration · September 30, 2026
- Affected product
- ARTIS pheno, ARTIS icono floor, ARTIS icono biplane, ARTIS icono
- Category
- Medical device recalls
- Hazard
- 30/09/2026 ARTIS pheno, ARTIS icono floor, ARTIS icono biplane, ARTIS icono ceiling with software version VE50B (only systems that were upgraded to VE50B) Medical Device Product Correction Class II Hospital
Check affected ARTIS pheno, ARTIS icono floor, ARTIS icono biplane, ARTIS icono identifiers →Therapeutic Goods Administration · September 30, 2026
- Affected product
- Various Procedure Packs containing BAG DRAWSTRING DUAL CORD 46X50CM
- Category
- Medical device recalls
- Hazard
- 30/09/2026 Various Procedure Packs containing BAG DRAWSTRING DUAL CORD 46X50CM Medical Device Recall Class II Hospital
Check affected Various Procedure Packs containing BAG DRAWSTRING DUAL CORD 46X50CM identifiers →Therapeutic Goods Administration · September 29, 2026
- Affected product
- Fibrase IM IV 100 mg/mL solution for injection, pack size 10
- Category
- Medical device recalls
- Hazard
- 29/09/2026 Fibrase IM IV 100 mg/mL solution for injection, pack size 10 ampoules x 1 mL Medicine Recall Class I Hospital
Check affected Fibrase IM IV 100 mg/mL solution for injection, pack size 10 identifiers →Therapeutic Goods Administration · September 29, 2026
- Affected product
- MultiFiltratePRO
- Category
- Medical device recalls
- Hazard
- 29/09/2026 MultiFiltratePRO Medical Device Product Correction Class II Hospital
Check affected MultiFiltratePRO identifiers →Therapeutic Goods Administration · September 29, 2026
- Affected product
- HemosIL AcuStar HIT-IgG(PF4-H). An in vitro diagnostic medical
- Category
- Medical device recalls
- Hazard
- 29/09/2026 HemosIL AcuStar HIT-IgG(PF4-H). An in vitro diagnostic medical device (IVD). Medical Device Recall Class II Hospital
Check affected HemosIL AcuStar HIT-IgG(PF4-H). An in vitro diagnostic medical identifiers →Therapeutic Goods Administration · September 29, 2026
- Affected product
- Fibrase (Pentosan) 100 mg/mL Injection (pack of 10 ampoules)
- Category
- Medical device recalls
- Hazard
- 29/09/2026 Fibrase (Pentosan) 100 mg/mL Injection (pack of 10 ampoules) Medicine Recall Class I Hospital
Check affected Fibrase (Pentosan) 100 mg/mL Injection (pack of 10 ampoules) identifiers →Therapeutic Goods Administration · September 28, 2026
- Affected product
- Centricity Enterprise Archive, Enterprise Archive, Centricity PACS
- Category
- Medical device recalls
- Hazard
- 28/09/2026 Centricity Enterprise Archive, Enterprise Archive, Centricity PACS, and Centricity PACS Server Medical Device Product Correction Class II Hospital
Check affected Centricity Enterprise Archive, Enterprise Archive, Centricity PACS identifiers →Therapeutic Goods Administration · September 28, 2026
- Affected product
- Arjo Carevo Shower Trolley
- Category
- Medical device recalls
- Hazard
- 28/09/2026 Arjo Carevo Shower Trolley Medical Device Product Correction Class II Consumer
Check affected Arjo Carevo Shower Trolley identifiers →Therapeutic Goods Administration · September 28, 2026
- Affected product
- NDI Passive Spheres 1,4,5,18 Spheres
- Category
- Medical device recalls
- Hazard
- 28/09/2026 NDI Passive Spheres 1,4,5,18 Spheres Medical Device Recall Class II Hospital
Check affected NDI Passive Spheres 1,4,5,18 Spheres identifiers →Therapeutic Goods Administration · September 28, 2026
- Affected product
- Nourex Professional Immune Defence 30 & 60 and Nourex Professional
- Category
- Medical device recalls
- Hazard
- 28/09/2026 Nourex Professional Immune Defence 30 & 60 and Nourex Professional Immune Force 30 & 60 Medicine Recall Class I Consumer
Check affected Nourex Professional Immune Defence 30 & 60 and Nourex Professional identifiers →Therapeutic Goods Administration · September 28, 2026
- Affected product
- F-18 Fludeoxyglucose
- Category
- Medical device recalls
- Hazard
- 28/09/2026 F-18 Fludeoxyglucose Medicine Recall Class III Hospital
Check affected F-18 Fludeoxyglucose identifiers →Therapeutic Goods Administration · September 28, 2026
- Affected product
- Buprenorphine Hydrochloride 0.3 mg/mL Injection (Pack of 5 x 1 mL
- Category
- Medical device recalls
- Hazard
- 28/09/2026 Buprenorphine Hydrochloride 0.3 mg/mL Injection (Pack of 5 x 1 mL Vials) Medicine Recall Class II Hospital
Check affected Buprenorphine Hydrochloride 0.3 mg/mL Injection (Pack of 5 x 1 mL identifiers →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 →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 →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 →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 →
