Medical Device Recalls
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1 result found
510(K) Number: K920736 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Lifeshield, latex-free Secondary I.V. Set, convertible pin, 32 inch, piggyback with OPTION-LOK, 15 d... | 2 | 04/15/2010 |
FEI # 3013319212 Hospira Inc. |
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