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Updated 2026-04-01

Orthalign, Inc recalls Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF

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Recalled Product

Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System

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Hazard / Issue

Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot # 25091103BB/ UDI: 00810832032427

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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