Alerts

Zimmer, in consultation with the TGA, has issued a hazard alert regarding its Natural-Knee II System metal-backed patella.

Consumers and health professionals are advised that Baxter Healthcare, in consultation with the TGA, is undertaking a recall for product correction of its HomeChoice Pro automated peritoneal dialysis system.

Medtronic Australasia has issued a hazard alert regarding multiple models of its neurostimulation devices, including those used for deep brain, spinal cord and peripheral nerve stimulation therapies.

Consumers and health professionals are advised that Medtronic Australasia has issued a hazard alert regarding multiple models of its spinal cord stimulation devices.

Medical Vision Australia Plastic & Cosmetic, has undertaken a recall of the implants and associated sizers.

Update - Recall now includes Papillon Mini blood glucose monitors.

List of all alerts for HomeChoice PRO automated peritoneal dialysis system recall.

Recall for product correction due to instructions for use update.

Recall due to higher flammability risk if washed incorrectly.

Medtronic Australasia has issued a hazard alert regarding two potential issues involving multiple models of its deep brain stimulation and spinal cord stimulation devices.

Medtronic Australasia has issued a hazard alert regarding two potential issues involving its SynchroMed II implantable infusion pump system.

Medtronic Australasia has issued a hazard alert for its Mosaic Porcine Aortic Bioprosthesis Model 305 due to the potential for implanting oversized valves.

Hazard alert due to software fault potentially leading to insufficient therapy.

Liko overhead lifts in chlorinated areas may have fastener corrosion, causing rails to fall. No reports in Australia but check your lifts and contact Hill-Rom for inspection.

Recall due to potential for incorrect blood glucose results.

Recall due to potential for protruding needles.

Recall due to replacement due to potential for breakdown.

Recall due to replacement due to potential for miscalibration.

Unlocated devices following recall for product correction.

Recall for product correction due to potential for aluminium tubing to break.

Recall for product correction due to potential for injury.