Medical Device Recalls
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1 result found
510(K) Number: K162059 |
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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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| GENICON EZEE Retrieval, sterile, Rx only. | 2 | 03/16/2018 |
FEI # 3002590791 Genicon, Inc. |
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