Medical Device Recalls
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1 result found
Recall Number: Z-2129-2018 |
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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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| Lapidus Plate, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Size/Step/Left or Right (Part Numbe... | 2 | 06/07/2018 |
FEI # 2183449 Orthofix, Inc |
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