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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Lifeshield, latex-free, Primary I.V. PLUMSET, convertible pin, 103 inch with backcheck valve, 2 CLAV... | 2 | 04/15/2010 | Hospira Inc. |
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