Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K052052 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Plum A+3 v.11.X, list #s 12618-04-01, 12918-04-03, 12618-04-05, 12618-04-51, 12618-04-07, 12618-04-5... | 2 | 10/06/2009 | Hospira Inc |
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