Medical Device Recalls
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1 result found
Recall Number: Z-1630-2026 |
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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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| Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System | 2 | 03/24/2026 |
FEI # 3007521480 Orthalign, Inc |
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