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Abbott Recalls HeartMate Touch System

The HeartMate Touch Communication System (version 1.0.32) is being recalled because the pump may unexpectedly stop or start. ....

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FDA Announces Abbott Recall of HeartMate Touch Communication System for Unintentional Pump Start and Stop

The U.S. Food and Drug Administration (FDA) announced that Abbott is recalling its HeartMate Touch System (version 1.0.32) for risk of unexpected pump stop or start. Issues may occur if the HeartMate Touch System is disconnected from a patient’s HeartMate Controller while a “pump stop” command is running. People who have the implantable HeartMate 3 Left Ventricular Assist Device may be affected. ....

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FDA Recalls 60,000 Abbott Pacemakers Due to Defect

Abbott’s SBP model pacemakers, sold under the Assurity and Endurity names, are being recalled because of the risk of electrical shorts. ....

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Class I Recall for Some Abbott Assurity and Endurity Pacemakers

Class I Recall for Some Abbott Assurity and Endurity Pacemakers
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