Orthofix U.S. LLC
4
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-07-22 to 2026-07-22
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-07-22 | FDA Device | FDA Recall: Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS REF: M111, Unilateral orthopedic/trauma exter | Orthofix U.S. LLC | Class II | N/A |
| 2026-07-22 | FDA Device | FDA Recall: Orthofix MINIRAIL, ARTICULATED, FIXATOR, VERTICAL AXIS REF: M122, Unilateral orthopedic/trauma exte | Orthofix U.S. LLC | Class II | N/A |
| 2026-07-22 | FDA Device | FDA Recall: Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number: M101, Unilateral orthopedic/trauma ext | Orthofix U.S. LLC | Class II | N/A |
| 2026-07-22 | FDA Device | FDA Recall: Orthofix MINIRAIL, SHORT, LENGTHENER REF: M103, Unilateral orthopedic/trauma external fixation devi | Orthofix U.S. LLC | Class II | N/A |