Alerts

Specific packs of Avaira Toric contact lenses are being recalled by CooperVision Australia Pty Ltd.

Avaira Toric contact lenses

About Octagam 5%: lifting of the voluntary recall

TRIAD Sterile Lubricating Jelly, 3g sachet, with lot numbers beginning with 7, 8, 9 or 0, is being recalled as it may not have been properly sterilised.

Product may not have been properly sterilised.

Recall of IGC Dorel Safety 1st Complete Healthcare Kit: Thermometer.

Kits with the above item number and barcode number contain a thermometer which displays the temperature reading in degrees Fahrenheit rather than degrees Celsius.

Recall of some LifeScan OneTouch Verio Blood Glucose Monitoring Systems

Users are experiencing repeated 'Error 2' warning messages when used in conditions of high temperature and/or humidity due to contamination on one of the meter's components, which occurred during the manufacturing process.

Minicrosser-Cyclone DX, 3- and 4-wheel mobility scooters, Models 130T & 140T, manufactured before January 2007, are being recalled.

There have been some instances in Europe where the controller on the subject units has spontaneously ignited due to a faulty controller setting.

The combination of products may not be suitable for use as a vehicle transport device.

Otto Bock Australia Pty Ltd has initiated a recall of a number of mobility chairs consisting of the combination of the Otto Bock Discovery Wheelbase and the Leckey Mygo Seat.

We are recalling Thelin (sitaxentan) worldwide due to serious liver risks. Consult your doctor if you have concerns.

Some cartons of Perindopril 2mg tablets labelled with batch numbers 24967, 24979, 25180, 25184 may contain Perindopril 8mg tablets

We have notified Johnson & Johnson Pacific that we are undertaking a consumer level recall of selected lots of 1-Day Acuvue TruEye contact lenses, as a precautionary measure.

Sponsor dispatched recall letters to all affected optometrists

Weight loss drug Sibutramine (Reductil) withdrawn in Australia due to heart risks.

The Therapeutic Goods Administration (TGA) has received enquiries about the recall of the LCS® DuofixTM Femoral Knee Replacement Component.

The Therapeutic Goods Administration (TGA) advises that Octapharma Australia Pty Ltd has agreed to a precautionary voluntary recall of all batches of Octagam intravenous immunoglobulin solutions from the Australian market.

Panvax Junior is being recalled because of a drop in potency, and all available stocks are being removed.

This batch of Survival Saline solution has been found to be contaminated and may cause infection.

Medical Visions Australia Pty Ltd following consultation with the Therapeutic Goods Administration is undertaking the recall of all non implanted silicone gel breast implants manufactured by Poly Implant Prothèse (PIP). The recall applies to all models of this type of implant.

Batch AR169 may contain AMLO 5 tablets (5mg amlodipine).