Alerts

The TGA advises health professionals and patients that Global Orthopaedic Technology has cancelled the Apex K2 Femoral Stem from the Australian Register of Therapeutic Goods (ARTG).

Data collected by the Australian National Joint Replacement Registry (NJRR) revealed that the SMR had a higher-than-expected revision rate.

Six batches of Infanrix hexa vaccine are being recalled due to potential contamination with Bacillus cereus. Consult your doctor if you have concerns.

Some batches of the Typhim Vi Vaccine are being recalled due to lower antigen content. Consult your doctor if you have concerns.

We are recalling Serenace (haloperidol) 0.5mg tablets from batch BJ431 due to mould contamination. Consult your doctor if you have concerns.

Poly Implant Prothèse (PIP) update

Poly Implant Prothèse (PIP) update

All lots of L-Gel Ultrasound Transmission Gel manufactured between June 2011 and May 2012 by Shanghai Shenfeng, China are being recalled.

List of all alerts regarding ABGII Modular Femoral Stem and Modular Neck - hip replacement system recall.

Poly Implant Prothèse (PIP) update

Therapeutic Goods Administration (TGA) advises that Stryker Australia Pty Ltd is recalling the ABGII Modular Femoral Stem and Modular Neck system used in hip replacements

Poly Implant Prothèse (PIP) update

Poly Implant Prothèse (PIP) update

Poly Implant Prothèse (PIP) update

Background information for consumers about Poly Implant Prothèse (PIP) breast implants

Poly Implant Prothèse (PIP) update

The Therapeutic Goods Administration (TGA) advises that the R3 metal liner component of the R3 acetabular system (used in hip replacements) is being recalled by the Australian sponsor, Smith & Nephew Surgical Pty Ltd.