Tyber Medical: Medical Device Recall in 2025 - (Recall #: Z-1221-2025)

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 LT- Medial Tibia Plate, 10-Hole, Left. Intended Fixation of fractures of the distal tibia Model/Catalog Number: 770715101

Product Classification:

Class II

Date Initiated: January 21, 2025

Date Posted: March 5, 2025

Recall Number: Z-1221-2025

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: 200 units

Code Information:

UDI-DI 00196449015993; Lot numbers 265814, 24060DF02, 24065DF03, 24060DF01. 24065DF05, 263512

Distribution Pattern:

Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated