Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K052735 |
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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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AlloCraft DBM with Syringe Assembly, 10 CC, LifeCell Corporation, Branchburg, NJ 08876 , Distribute... | 3 | 03/26/2008 | LifeCell Corporation |
AlloCraft DBM with Syringe Assembly, 5CC, Catalog/Reorder Number: 653005, LifeCell Corporation, Bran... | 3 | 03/26/2008 | LifeCell Corporation |
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