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AU recall: ITL Australia catheter kit - compromised sterility of specific models/lots

Recall in Australia of specific models and lots of this single-use surgical procedure pack due to possible compromised sterility, increasing the risk of patient bloodstream infection.

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AU defect: Philips IntelliVue Monitors with Nellcor SpO2 Boards, malfunction with age

The SpO2 function on certain model numbers deteriorates with age, leading to a malfunction technical alarm. Keep an alternative SpO2 monitor on hand, and book a service if malfunction occurs.

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Probable allergic reaction to Spongostan

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

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Product Defect Alert: Pressure Plates used in Level 1 Fast Fluid Flow Fluid Warmers

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.

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AU recall: Philips BiPAP A40 – non-conforming materials could cause off-gassing or device failure

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.

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Recall: ISO-GARD filter for breathing circuits (antimicrobial heat-moisture exchanger) may split or

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.

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Neural connector (NRFit®) changeover

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

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Mortality Sub-committee

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...

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Patient experience survey (anaesthesia) - guideline

Patient experience survey (anaesthesia) - guideline

Class 1 recall notification - Infusion Sets for Alaris™ Pumps (GP, VP, CC, GW/GW800, SE and IVAC™ 59

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

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