Recall in Australia of bi-level positive airway pressure (BiPAP) ventilator devices that may contain a plastic material that could degrade and cause off-gassing or device failure.

The college has been made aware of an incident involving a probable allergic reaction to Spongostan (a gelatin foam).

A changed hinge design may cause variable pressure on the IV bag, leading to under-delivery or delay of therapy with possible consequences including hypothermia, hypovolemia, and/or hypotension.

Specified lot numbers of ISO-GARD filters marketed by Teleflex Medical may split or detach during use, potentially resulting in leakage and insufficient air supply. Check for affected stock, quarantine and return.

Important information about the introduction of neural devices with connectors compliant with the new international standard ISO 80369-6.

The Mortality Sub-committee was developed as a collaboration between the chairs of established anaesthetic mortality committees in Australia, under the auspices of ANZCA. The group is chaired by Dr Simon Jenkins, and includes the chairs of all established anaesthetic mortality...

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

Manufacturer, Becton Dickinson (BD), has advised of the recall of a number of Dedicated and Non–dedicated infusion sets and accessories.

Following the death of a person after minor foot surgery, ANZCA reminds fellows that under certain conditions the interaction of gabapentinoids and opioids can cause severe respiratory depression, resulting in death.