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US FDA classifies recall of Abiomed's blood pumps as most serious
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US FDA classifies recall of Abiomed's blood pumps as most serious
Mar 21, 2024 8:13 AM

March 21 (Reuters) - The U.S. health regulator on

Thursday classified the recall of some Impella Left Sided Blood

Pumps by Abiomed, a Johnson & Johnson ( JNJ ) company, as the

most serious and said that its use could cause serious injuries

or death.

(Reporting by Bhanvi Satija in Bengaluru; Editing by Anil

D'Silva)

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