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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

- The U.S. health regulator on Thursday classified the recall of some Impella Left Sided Blood Pumps by Abiomed, a Johnson & Johnson JNJ.N 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)

((Bhanvi.Satija@thomsonreuters.com; Outside U.S. +91 9873062788;))

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