FDAJanuary 21, 2025device

A.L.P.S. mvX- MEDIAL TIBIA PLATE 10H LT- Medial Tibia Plate, 10-Hole, Left. Intended Fixation of fractures of the distal tibia Model/Catalog Number: 770715101

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

What to do

FDA enforcement status: Ongoing

Brands named

tyber medicaltyber

UPCs

00196449015993

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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