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Getinge Recalls Vaporizer Sevoflurane Maquet Filling for Risk of Patient and Health Care Professional Exposure to Toxic Chemical Hydrogen Fluoride

Vaporizer Sevoflurane Maquet Filling is part of the Flow anesthesia systems but may expose patients or health professionals to toxic hydrogen fluoride.

http://www.fda.gov/medical-devices/medical-device-recalls/getinge-recalls-vaporizer-sevoflurane-maquet-filling-risk-patient-and-health-care-professional

 
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Teleflex/Arrow International Recall Arrow FiberOptix and UltraFlex Intra-Aortic Balloon (IAB) Catheter Kits for Manufacturing Issue That May Prevent Full Balloon Inflation and Cause Patient Harm

Arrow FiberOptix and UltraFlex IAB Catheter Kits provide circulatory support. A manufacturing issue may prevent the balloon from fully inflating.

http://www.fda.gov/medical-devices/medical-device-recalls/teleflexarrow-international-recall-arrow-fiberoptix-and-ultraflex-intra-aortic-balloon-iab-catheter