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Recall Observatory FDA recall evidence

Device product

A.L.P.S. mvX - ANATOMIC LAT FIB PLATE 4H LT: Anatomic Lateral Fibula Plate, 4-hole, Left Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770708041

Z-1209-2025

January 21, 2025

Class II

Product summary

Firm
Tyber Medical
Event
Event 96212
Status
Ongoing
Classification
Class II
Quantity
412 units
Official record key
device-enforcement:Z-1209-2025

Official wording

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 information: UDI-DI; 00196449015528 Lot Numbers 24043BU03, 267844, 24043BU02, 261286

Distribution pattern: Nationwide

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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