FDA Enforcement Class II Ongoing

A.L.P.S. mvX- Product Name: ANATOMIC LAT FIB PLATE 10H LT Anatomic Lateral Fibula Plate, 10-Hole, Left. Intended Fixation of fractures of the distal tibia Model/Catalog Number: 770708101

Recall: Z-1215-2025 · Reported March 5, 2025

Enforcement

Recall Number
Z-1215-2025
Event ID
96212
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Tyber Medical
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
March 5, 2025
Initiation Date
January 21, 2025
Classification Date
February 21, 2025
Address
83 S Commerce Way Ste 310, N/A, Bethlehem, PA, 18017-8934, United States

Description

A.L.P.S. mvX- Product Name: ANATOMIC LAT FIB PLATE 10H LT Anatomic Lateral Fibula Plate, 10-Hole, Left. Intended Fixation of fractures of the distal tibia Model/Catalog Number: 770708101

Reason

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

Code Info

UDI-DI 00196449015580; Lot Numbers 269171, 265809, 262558, 260891

Distribution

Nationwide

Quantity

220 units