Medical Device Recalls
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1 result found
510(K) Number: K011925 |
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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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| Portex Hypodermic Needle-Pro Syringe and Needle 1ml/LS Small Gauge Safety 27 g x 1/2'' Reference Nu... | 2 | 07/20/2004 |
FEI # 1217052 Smiths Medical ASD, Inc. |
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