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10 major recalls in 60 days: What ASCs need to know

In the last 60 days, 10 major device and medication recalls have potentially put patients at risk across ASCs and hospitals nationwide. Learn more about the rec

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Getinge s cardiac device sees 5th recall notice in 2023

About 16,000 Getinge Cardiosave Hybrid and Rescue Intra-aortic Balloon Pumps have been recalled due to risks of the balloon breaking, power failures and circuit board communication failures.

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Datascope/Maquet/Getinge Recalls Cardiosave Hybrid and Rescue Intra-aortic Balloon Pumps (IABPs) for Unexpected Shutdowns

The FDA has announced that Datascope/Maquet/Getinge is recalling the Cardiosave Hybrid and Rescue Intra-aortic Balloon Pumps (IABPs) because they may shutdown unexpectedly due to electrical failures in the Power Management Board and/or Solenoid Board (Power Source Path).

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Another FDA Class I Recall of Cardiosave Hybrid/Rescue IABPs

The 4586 recalled Cardiosave Hybrid/Rescue intra-aortic balloon pumps may shutdown unexpectedly due to electrical failures in the power source path, leading to serious harm.

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Cardiosave Intra-Aortic Balloon Pumps Recalled Due to Battery Failure

Maquet received 6 reports of battery failure but believes this might be under reported

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