fda
4 records
FDA Recall: Orthalign, Inc — Class II
20260401
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm) | Product: Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Kne...
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FDA Recall: Orthalign, Inc — Class II
20260401
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm) | Product: Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee...
View Source
FDA Device Recall: Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component L
2026-04-01
Class II — Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
View Source
FDA Device Recall: Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component La
2026-04-01
Class II — Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
View Source
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