Abiomed Recalls Impella 5.5 Left Ventricular Device Systems: Urgent Action Required to Address Product Leakage
Abiomed has issued a class I recall for specific Impella 5.5 left ventricular device systems, citing product leakage. The urgent recall highlights potential risks to patients, urging immediate action to address the issue and prevent serious injuries or death. Abiomed reported 179 complaints and three injuries related to the recall.
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