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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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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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PG68(A) Guideline surgical patient safety SARS-CoV-2

To provide frequently updated advice on safety concerns for surgery in patients with current or previous SARS-CoV-2 infection, or who have recently received or soon plan to receive a SARSCoV-2 vaccination

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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Practice without direct patient care toolkit

Practice without direct patient care toolkit

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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Co-prescription of gabapentinoids and opioids

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.

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Jannsen-Cilag CADD Infusions Systems Disposables product defect

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

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Product defect correction: damaged barrels on BD Plastipak 50mL Syringe with Luer-Lok Tip

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

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