Alerts

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.

Recall for product correction due to potential for handle to break.

Recall due to replacement with newer model.

A hazard alert has been issued to cardiologists and surgeons regarding some models of Cognis Cardiac Resynchronisation Therapy Defibrillators (CRT-Ds) and Teligen Implantable Cardioverter Defibrillators (ICDs).

Hazard alert due to updated surgical instructions and additional quality check.

Consumers and health professionals are advised that LMT Surgical is issuing a hazard alert for all sizes and lots of its PyroTitan humeral resurfacing arthroplasty device.

It has been identified that there is a potential for some screws from the affected lot to break during insertion or removal.

Consumers and health professionals are advised that Aimedics, in consultation with the TGA, is recalling from the market all units of its HypoMon sleep-time hypoglycaemic monitor.

Zimmer is recalling from the market for the purpose of relabelling unused stock of its NexGen micro implants.

Boston Scientific has initiated a recall for product correction for multiple lots of its Promus Element Plus Monorail everolimus-eluting coronary stent system.

Novo Nordisk Pharmaceuticals has initiated a recall for product correction of certain lots of its NordiPen medical device.

Recall due to potential gas leak.

Stryker Australia has issued a hazard alert to surgeons regarding its Oasys Midline Occipital Plate.

Recall for product correction for Medtronic SynchroMed II and SynchroMed EL implantable infusion pumps.