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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
Related Medical Device Recalls Recall Date to: 07/01/2015
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Product Description
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FDA Recall
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Z-1230-2014 - Heart Mate II Pocket Controllers removed from packaging Product Usage: HeartMate II is a mechanical device that circulates blood throughout the body when the heart is too weak to pump blood adeq... 1 03/21/2014 Thoratec Corporation
Z-1227-2014 - HeartMate II Implant Kit with Pocket Controller; with sealed grafts (NAm) with sealed grafts (EU) Product Usage: HeartMate II is a mechanical device that circulates blood throughout the body whe... 1 03/21/2014 Thoratec Corporation
Z-229-2014 - HeartMate II LVAD Pump and Pock Controller Kit; Product Usage: HeartMate II is a mechanical device that circulates blood throughout the body when the heart is too weak to pump blood adequately o... 1 03/21/2014 Thoratec Corporation
Z-1228-2014 - HeartMate II System Controller Product Usage: HeartMate II is a mechanical device that circulates blood throughout the body when the heart is too weak to pump blood adequately on its own. It is so... 1 03/21/2014 Thoratec Corporation
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