Alerts

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

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

Consumers and health professionals are advised that Coloplast, in consultation with the TGA, has undertaken a recall for product correction for its Peristeen anal irrigation system.

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.

St Jude Medical Australia has issued a hazard alert regarding its Implantable Cardiac Devices (ICDs, including Cardiac Resynchronisation Therapy Defibrillators (CRT-Ds)) when reprogrammed with the Merlin Programmer using software version 17.2.2.

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

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.

Owners and people responsible for HeartSine PAD 300/PAD 300P public access defibrillators are advised that Aero Healthcare, in consultation with the TGA, undertook a recall for product correction of some of these devices in November 2012 to correct certain battery and software problems that may affect the ability of the device to work in the event it is needed.

Ausmedic Australia is undertaking a recall for product correction for certain models of Viper and Viper Plus powered wheelchairs

Consumers and health professionals are advised that Hill-Rom, in consultation with the TGA, is undertaking a recall for product correction for the Liko Standard SlingBar 450.

Consumers and health professionals are advised that Mobility Plus, in consultation with the TGA, is undertaking a recall for product correction of Crocodile size 3 walkers.

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).

Stryker Australia, in consultation with the TGA, has issued a hazard alert to surgeons regarding OtisMed ShapeMatch Cutting Guides.