Tyber Medical: Medical Device Recall in 2025 - (Recall #: Z-1222-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

A.L.P.S. mvX-MEDIAL TIBIA PLATE 10H RT-Medial Tibia Plate, 10-Hole, Right Intended Fixation of fractures of the distal tibia. Model/Catalog Number: 770715102

Product Classification:

Class II

Date Initiated: January 21, 2025

Date Posted: March 5, 2025

Recall Number: Z-1222-2025

Event ID: 96212

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

Status: Ongoing

Product Quantity: 209 units

Code Information:

UDI-DI 00196449016006; Lot Numbers 265815, 24055DF03, 24055DF04

Distribution Pattern:

Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated