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Cardiosave Hybrid and Cardiosave Rescue IABPs Recalled Due to Reports of Fluid Leaks

Cardiosave Hybrid and Cardiosave Rescue IABPs Recalled Due to Reports of Fluid Leaks
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FDA Class I Recall of CardioSave Hybrid/Rescue IABPs

Subpar batteries that do not meet performance specifications were mistakenly released to a limited number of customers and may have a shortened run-time and fail unexpectedly. ....

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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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Class I Recall of Batteries for Cardiosave Hybrid/Rescue IABPs: FDA

Class I Recall of Batteries for Cardiosave Hybrid/Rescue IABPs: FDA
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