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U.S. Department of Health and Human Services

Medical Device Recalls
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71 to 80 of 150 Results
Recall Date to: 10/07/2015 510(K) Number: K022947
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100/120V 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: 100/120V AC, Advanced Perfusion System 1 The Terumo® Advance... 2 08/14/2013 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 (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
Terumo Advanced Perfusion System 1 Flow Module indicated for use in extracorporeal circulation of... 2 09/25/2012 Terumo Cardiovascular Systems Corporation
Terumo Advanced Perfusion System 1 ASSEMBLY FLOW POD Product Usage: The Terumo Advanced Perfusion... 2 09/24/2012 Terumo Cardiovascular Systems Corporation
Interface module for CDl System 100/101 Product Usage: The Interface Module for CDl 500 is the i... 2 08/21/2012 Terumo Cardiovascular Systems Corporation
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