Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K053000 |
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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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Haemonetics cardioPAT -Cardiovascular Perioperative Autotransfusion System Model 2050 US Models Ou... | 2 | 08/05/2011 | Haemonetics Corporation |
Haemonetics cardioPAT Cardiovascular - autotransfusion System Catalog Number: 02050-US | 2 | 02/22/2011 | Haemonetics Corporation |
Haemonetics cardioPAT System, Product List Number 02050, Haemonetics Corporation, Braintree, MA 0218... | 2 | 12/08/2007 | Haemonetics Corporation |
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