Alerts

CSL Biotherapies is recalling the batch 3450700309 of Albumex 4, due to the presence of ethylene glycol

Some batches of Albumex manufactured prior to 25 January 2012 may be contaminated with very low levels of ethylene glycol

Information on the management of issues related to the recall of PIP silicone gel breast implants

Information on the management of issues related to the recall of PIP silicone gel breast implants

The TGA advises that while PIP breast implants were recalled due to the use of unauthorised silicone, current evidence does not support routine removal in patients without symptoms, and individuals are encouraged to seek medical advice if concerned.

At the time of writing, the TGA has been advised that approximately 9,054 PIP breast implants have been implanted by surgeons between 2002 and 2010. In April 2010 non-implanted PIP breast implants were recalled from the Australian marketplace.

Specific lots of an additional contact lens model i.e. Avaira Sphere Contact Lens have been identified as being affected by the unintended presence of a residue identified as silicone oil.

Specific packs (lots) of Avaira Sphere contact lenses are being recalled by CooperVision Australia Pty Ltd

We are recalling all batches of Savacol Antiseptic Mouth & Throat Rinse (alcohol-free) due to bacterial contamination.

Xigris (drotrecogin alfa) is being withdrawn from the market because it does not improve survival rates in severe sepsis patients. Stop using it and consult your doctor for alternative treatments.

The Therapeutic Goods Administration (TGA) has been advised by Ferno Australia Pty Ltd that a small number of Meducore Easy Automatic External Defibrillator (AEDs) that are currently being recalled for product correction cannot be located.

This is an update to the alert issued by the TGA on 16 June 2011. Johnson and Johnson have advised the TGA of additional serial numbers affected by the recall.

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

About Octagam 5%: lifting of the voluntary recall

The Therapeutic Goods Administration (TGA) has been advised that 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.