Fresh Recalls

Orthofix U.S recalls

4 recent recalls on record for Orthofix U.S in connected official government data as of October 22, 2026 at 6:00 PM UTC.

Models with recalls

Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS REF (1)Orthofix MINIRAIL (3)

All Orthofix U.S recalls

FDA Class II · Medical device · July 22, 2026

Orthofix MINIRAIL recall — Orthofix U.S. LLC

Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111

Official ID Z-2732-2026 · Official record ↗

FDA Class II · Medical device · July 22, 2026

Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS REF recall — Orthofix U.S. LLC

Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111

Official ID Z-2731-2026 · Official record ↗

FDA Class II · Medical device · July 22, 2026

Orthofix MINIRAIL recall — Orthofix U.S. LLC

Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111

Official ID Z-2730-2026 · Official record ↗

FDA Class II · Medical device · July 22, 2026

Orthofix MINIRAIL recall — Orthofix U.S. LLC

Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111

Official ID Z-2729-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.