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.

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...

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.

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.