Class II

Medical Device Recall: A.L.P.S. mvX-MEDIAL TIBIA PLATE 6H LT-Medial Tibia Plate, 6-Hole, Left Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770715061

Tyber Medical · January 21, 2025

Reason for Recall

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

Distribution

Nationwide

States Affected

NATIONWIDE

Quantity Affected

197 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1219-2025

Status: ongoing

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