Damaged barrels may admit air. Check all devices before, during and after use, and report any defective devices discovered.

Several of the eight issues could cause serious injury or death. Remove and quarantine device from use.

Recall in Australia of certain lot numbers of Medtronic endotracheal tubes, after a shipment may have been exposed to fungicide.

Breached seal in packaging of specific lot numbers of these wire guide devices means sterility is compromised, creating risk of infection in patients. Quarantine all unused devices and return to supplier.

A recall has been issued for batches J036913AA & J036913BA of DBL Vancomycin (vancomycin hydrochloride) 500 mg powder for injection vials due to out of specification of specificity stability results which do not meet the shelf-life specification for potency or have atypically...

Jannsen-Cilag CADD Infusion Systems Disposables as part of Veletri Consumables Kit may underdeliver infusion doses or fail to detect attachment of the cassettes.

Patient experience survey (anaesthesia) - guideline

In May 2023, the TC-RGA agreed that Rural Generalist Anaesthetists (RGAs) would be recommended to undertake the Continuing Professional Developement (CPD) program-level requirements identified in the ANZCA and FPM CPD standard.

We oversee a range of incident reporting activities in Australia and New Zealand, including mortality reporting and webAIRS, to ensure that we continue to be two of the safest countries in the world to undergo anaesthesia.

Our professional documents, statements and guidelines are crucial for promoting the safety and quality of patient care for those undergoing anaesthesia for surgical and other procedures and for those receiving pain medicine treatment.