Medical Device Recalls
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141 to 146 of 146 Results
Recall Date to: 04/16/2014 510(K) Number: K022947 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Terumo® Advanced Perfusion System 1 (APS1, System 1) 100/120V AC Product Usage: The Terumo® Adv... | 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: 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 |
220/240V AC, Advanced Perfusion System 1 Product Usage: The Terumo® Advanced Perfusion System 1 ... | 2 | 08/15/2013 | 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 |
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