Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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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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| Z-0795-2007 - Gynecare PROLIFT Total Pelvic Repair System PFRT01 Ethicon Deutschland | 2 | 05/10/2007 |
FEI # 2210968 Ethicon, Inc. |
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