Recall Alert: FDA Abbott & Thoratec Pull 14,000 HeartMate LVADs Over Safety Concerns

Chicago, Illinois – The U.S. Food and Drug Administration (FDA) has issued a Class I recall for nearly 14,000 HeartMate left ventricular assist devices (LVADs) manufactured by Abbott and its subsidiary Thoratec. This recall comes after continued concerns over safety that have been linked to multiple deaths associated with the devices. The recall specifically pertains … Read more