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HeartMate 3 Recalled for Risk of Blood Leaks or Air in System

HeartMate 3 Recalled for Risk of Blood Leaks or Air in System
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Abbott Thoratec , Drug Administration , Abbott Thoratec Corporation , Thoratec Corporation , Urgent Medical Device Correction Notification ,

HeartMate II and 3 LVADs Recalled Due to Potential for Outflow Graft Obstruction

Initiated by Abbott/Thoratec and deemed Class I by the FDA, the recall is a response to reports of 273 injuries and 14 deaths. ....

Drug Administration , Abbott Thoratec Corporation , Thoratec Corporation , Urgent Medical Device Correction Letter ,