Tyber Medical: Medical Device Recall in 2025 - (Recall #: Z-1223-2025)

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 12H LT-Medial Tibia Plate, 12-Hole, Left Intended forFixation of fractures of the distal tibia Model/Catalog Number: 770715121

Product Classification:

Class II

Date Initiated: January 21, 2025

Date Posted: March 5, 2025

Recall Number: Z-1223-2025

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: 201 units

Code Information:

UDI-DI 00196449016013; Lot Numbers 265816, 24064DF01, 263557, 24065DF04, 24059DF03, 24059DF02

Distribution Pattern:

Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated