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Arrow International, LLC, subsidiary of Teleflex, Inc Recalls Arrow AutoCAT 2, AC3 Intra-Aortic Balloon Pumps for Unexpectedly Short Battery Run Times

Batteries on the Arrow AutoCAT 2 and AC3 Intra-Aortic Balloon Pumps deplete faster than expected, which may cause the pump to stop during patient transport.

http://www.fda.gov/medical-devices/medical-device-recalls/arrow-international-llc-subsidiary-teleflex-inc-recalls-arrow-autocat-2-ac3-intra-aortic-balloon

 
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Whele LLC Recalls Mighty Bliss Electric Heating Pads Due to Injury Risks Including Electric Shocks, Skin Burns, and Rashes

Mighty Bliss electric heating pads are being recalled because they may cause injuries including electric shocks, burns, rashes and irritation.

http://www.fda.gov/medical-devices/medical-device-recalls/whele-llc-recalls-mighty-bliss-electric-heating-pads-due-injury-risks-including-electric-shocks-skin

 
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Teleflex and Arrow International, LLC Recall Arrow MAC Two-Lumen Central Venous Access and Pressure Injectable Arrowg+ard Blue Plus Three-Lumen Central Venous Catheter (CVC) Kits

An inadequate connection between housings in Arrow multi-lumen central venous access and catheter kits may cause a cross lumen leak that can harm patients.

http://www.fda.gov/medical-devices/medical-device-recalls/teleflex-and-arrow-international-llc-recall-arrow-mac-two-lumen-central-venous-access-and-pressure