Medical Device Recalls
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1 result found
Recall Number: Z-1222-2025 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| A.L.P.S. mvX-MEDIAL TIBIA PLATE 10H RT-Medial Tibia Plate, 10-Hole, Right Intended Fixation of frac... | 2 | 02/21/2025 |
FEI # 3012966183 Tyber Medical |
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