Reports of Injuries, Deaths Prompt FDA to Recall Heart Failure Devices

WEDNESDAY, April 17, 2024 -- The HeartMate II and HeartMate 3, manufactured by Thoratec Corp., a subsidiary of Abbott Laboratories, are now under a strict U.S. Food and Drug Administration recall after being tied to 273 known injuries and 14...
Source: Drugs.com - Pharma News - Category: Pharmaceuticals Source Type: news