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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2023-RGA-SSSA-Examination-Report
2023 RGA SSSA Examination Report
Two product defect corrections: Medtronic NIM EMG Endotracheal Tubes
Cuff overinflation hazard, and manufacturing fault in specific production lots causing electronic malfunction.
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Safety issue with self-inflating resuscitation bag
During an emergency situation involving the use of a self-inflating resuscitation bag-valve-mask unit, the mask could not be readily detached, which prevented connection to the laryngeal mask/endotracheal tube.
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Case discussion/conferencing guideline
Case discussion/conferencing guideline
Multi-source feedback (pain medicine) - self-assessment form
Multi-source feedback (pain medicine) - self-assessment form
Multi-source feedback (pain medicine) - summary form
Multi-source feedback (pain medicine) - summary form
Multi-source feedback (procedures in pain medicine) - self-assessment form
Multi-source feedback (procedures in pain medicine) - self-assessment form
Multi-source feedback (procedures in pain medicine) - summary form
Multi-source feedback (procedures in pain medicine) - summary form
PS04(A)BP Position statement on the post-anaesthesia care unit Background Paper
PS04(A)BP Position statement on the post-anaesthesia care unit Background Paper