US FDA classifies recall of Abiomed's blood pumps as most serious
Reuters · 03/21 14:46
US FDA classifies recall of Abiomed's blood pumps as most serious
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.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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