Alerts

Maxman IX Capsules pose a serious risk to your health and should not be taken. They contain undeclared sildenafil and have not been assessed for quality, safety or efficacy.

Medtronic has initiated a recall of unused stock of multiple lots of its Infuse/LT-Cage Bone Graft Kit.

Medtronic has initiated a recall for product correction for its Medtronic Paradigm insulin infusion sets.

The TGA advises that GNY Australia has initiated a recall of GNY Slimming Pills - labelled as MSV (Strong Version), ESV (Extra Strong Version) and GRL (Rapid Loss Soft Gel Capsules) - as they pose a serious health risk.

Johnson & Johnson Medical is issuing a hazard alert to implanting surgeons regarding one lot of its Glenosphere Orientation Guide (lot number 5120443).

Yong Gang tablets pose a serious risk to your health and should not be taken. They contain undeclared tadalafil and sildenafil and have not been assessed for quality, safety or efficacy.

MMC Maxman V capsules pose a serious risk to your health and should not be taken. The contain undeclared sildenafil and phenolphthalein, which has serious safety concerns.

TGA safety alert on cyproterone + ethinyloestradiol products (e.g. Diane‑35) highlights an increased risk of blood clots, advising careful patient selection while noting benefits outweigh risks when used as approved.

Johnson & Johnson Medical has initiated a recall of all unused stock and issued a hazard alert to implanting surgeons for two Codman Certas Programmable Valve products.

The TGA has issued updated safety advice for health professionals regarding dabigatran (Pradaxa), highlighting the increased risk of bleeding and the importance of careful patient selection and monitoring, especially in older adults and those with kidney impairment.

TGA has issued updated safety advice for consumers taking Pradaxa (dabigatran), highlighting risks such as bleeding and the importance of proper storage and patient monitoring.

Gardasil is a vaccine that protects males and females from a range of cancers (including cervical and anal cancers) and other diseases caused by human papillomavirus (HPV). It is administered as three injections over six months.

Health professionals and consumers are advised that Roche Diagnostics Australia, after consultation with the TGA, has initiated a recall for product correction for its CoaguChek XS, CoaguChek XS Plus and CoaguChek XS Pro INR monitors.

Beast Amphetalean powder poses a serious health risk and should not be taken. It contains prescription yohimbine, alpha‑yohimbine and DMAE, is unapproved, and includes a prohibited import.

Yixiu L-Carnitine Slimming capsules pose a serious health risk and should not be taken. They contain undeclared sibutramine. This increases the risk of major cardiac events.

TGA safety alert for Aurum Adrenaline 10 mL 1:10,000 pre‑filled syringes warns of label misalignment that may create the appearance of overfill, posing a risk of dosing errors and requiring cautious use.

BSN Hyper Shred capsules pose a serious health risk and should not be taken. They contain prescription-only oxedrine. Health risks may seriously increase if taken with interacting drugs.

Mojo Risen capsules pose a serious risk to your health and should not be taken. They contain undeclared tadalafil and have not been assessed for quality, safety or efficacy.

Ziyinzhuangyang tablets pose a serious risk to your health and should not be taken. They contain undeclared sildenafil and have not been assessed for quality, safety or efficacy.

Maxman III capsules pose a serious risk to your health and should not be taken. They contain undeclared sildenafil and have not been assessed for quality, safety or efficacy.

Health professionals and consumers are advised that Abbott Diabetes Care, after consultation with the TGA, has initiated a recall for product correction for its FreeStyle InsuLinx Blood Glucose Meter.

Health professionals and consumers are advised that Alcon Laboratories Australia, in consultation with the TGA, has issued a hazard alert regarding AcrySof Cachet Phakic Lenses.

Health professionals and consumers are advised that Johnson & Johnson Medical Pty Ltd, after consultation with the TGA, is recalling its OneTouch Verio IQ Blood Glucose Meter.

Health professionals and consumers are advised that Hoya Surgical Optics, in consultation with the TGA, is recalling certain Hoya One-Piece Intraocular Lenses (IOLs) that are in the supply chain.

Health professionals and consumers are advised that selected lots of AMS 800 Control Pumps may not function as intended by the manufacturer, American Medical Systems Inc (AMS).