The FDA has disclosed over 60 additional safety reports relating to intra-aortic balloon pumps manufactured by Maquet and Datascope, including two patient deaths, following a Class I recall this past ...
Two deaths, one serious injury and more than 60 medical device reports have been linked to Maquet/Datascope’s intra-aortic balloon pumps in the past year, the FDA warned healthcare providers in a Nov.
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