Medical Device Recalls
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1 result found
510(K) Number: K921365 |
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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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| Nutrimix Micro Compounder, List #s 11365-04-01, 11365-04-03, 11365-04-05; AC cord manufactured by El... | 2 | 10/06/2009 |
FEI # 2921482 Hospira Inc |
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