Medical Device Recalls
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1 result found
510(K) Number: K043127 |
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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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cardioPAT Cardiovascular Perioperative Autotransfusion System, Model: LN 2050-110-E and Disposables... | 2 | 11/23/2005 | Haemonetics Corporation |
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