Monday, June 19, 2017

Datascope Corp/MAQUET Issues Worldwide Voluntary Recall of the System CS100, CS100i and CS300 Intra-Aortic Balloon Pumps for Potential Electrical Test Failure Code - FDA Safety Alerts & Drug Recalls

Datascope Corp. is voluntarily performing a worldwide field correction of certain Intra-Aortic Balloon Pumps (IABPs) sold by Datascope Corp. for a potential electrical test failure code.

from Food and Drug Administration--Recalls/Safety Alerts http://ift.tt/2sOBU1J
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