Medical Device Recalls
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41 to 41 of 41 Results
510(K) Number: K881330 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Smart Perfusion Pack, REF: 086500301, Sterile EO, Sorin Group USA, Inc., 14401 W. 65th Way, Arvada, ... | 2 | 03/12/2010 | Sorin Group USA, Inc. |
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