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Cardiosave IABPs—Yet Again—the Subject of a Class I Recall: FDA

Just 7 days after issuing a previous alert, the agency is pointing to another problem that could cause unexpected device shutdowns.

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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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Getinge subsidiary Datascope has another aortic pump recall

The FDA issued a notice labeling another recall of Getinge subsidiary Datascope's Cardiosave pump as Class I, the most serious kind.

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FDA designates recall of two intra-aortic balloon pumps as class I

FDA designates recall of two intra-aortic balloon pumps as class I
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Cardiosave IABPs Recalled Again, This Time Due to Potential Electrical Problems: FDA

The beleaguered company is pulling the pumps due to electrical failures in the power management or solenoid boards.

Datascope maquet getingeDrug administrationCardiosave hybridCardiosave rescue

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