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FDAFDA · Food and drugs·Recall number Z-1212-2025

A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 6H RT: Anatomic Lateral Fibula Plate, 6-hole, Right Model/Catalog Number: 770708062

Published March 5, 2025 · Recall initiated: January 21, 2025

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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

What to do

Voluntary: Firm initiated · E-Mail

Recall details

Manufacturer
Tyber Medical
Distributor
Nationwide
Lot
UDI-DI 00196449015559; Lot Numbers 265783, 267847, 24036BU02, 261289
Risk classification
Class II
Area (FDA)
device
Country
United States

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