Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Z-1629-2026 - Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System | 2 | 03/24/2026 |
FEI # 3007521480 Orthalign, Inc |
| Z-1630-2026 - 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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