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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 148 Results
Recall Date to: 11/28/2014 510(K) Number: K022947
 
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Terumo® Advanced Perfusion System 1 220/240V AC, Advanced Perfusion System Platform (APS) 2 07/08/2014 Terumo Cardiovascular Systems Corporation
Terumo® Advanced Perfusion System 1 100/120V AC, Advanced Perfusion System Platform (APS) 2 07/08/2014 Terumo Cardiovascular Systems Corporation
100/120V AC, Advanced Perfusion System 1 Product Usage: The Terumo® Advanced Perfusion System 1 ... 2 08/15/2013 Terumo Cardiovascular Systems Corporation
220/240V AC, Advanced Perfusion System 1 Product Usage: The Terumo® Advanced Perfusion System 1 ... 2 08/15/2013 Terumo Cardiovascular Systems Corporation
Terumo® Advanced Perfusion System 1: 220/240V AC, Advanced Perfusion System 1 The Terumo® Advanc... 2 08/14/2013 Terumo Cardiovascular Systems Corporation
Terumo® Advanced Perfusion System 1: 100/120V AC, Advanced Perfusion System 1 The Terumo® Advance... 2 08/14/2013 Terumo Cardiovascular Systems Corporation
Terumo® Advanced Perfusion System 1 (APS1, System 1) Description: 220/240V AC Product Usage: Th... 2 08/14/2013 Terumo Cardiovascular Systems Corporation
Terumo® Advanced Perfusion System 1 (APS1, System 1) 100/120V AC Product Usage: The Terumo® Adv... 2 08/14/2013 Terumo Cardiovascular Systems Corporation
100/120V AC, Advanced Perfusion System Platform (APS) The Terumo® Advanced Perfusion System 1 is ... 2 11/27/2012 Terumo Cardiovascular Systems Corporation
220/240V AC, Advanced Perfusion System Platform (APS) The Terumo® Advanced Perfusion System 1 is ... 2 11/27/2012 Terumo Cardiovascular Systems Corporation
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