Medical Device Recalls
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1 result found
510(K) Number: K032040 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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SYNERGY Perfusion Tubing Systems US Denver PHISIO, Sorin Group USA, Tubing set heart-lung bypass, St... | 2 | 01/14/2012 | Sorin Group USA, Inc. |
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