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Recall Observatory FDA recall evidence

Device product

A.L.P.S. mvX-P: ANATOMIC LAT FIB PLATE 12H LT- Anatomic Lateral Fibula Plate, 12-Hole, Left. Inended for Fixation of fractures of the distal tibia Model/Catalog Number: 770708121

Z-1217-2025

January 21, 2025

Class II

Product summary

Firm
Tyber Medical
Event
Event 96212
Status
Ongoing
Classification
Class II
Quantity
100 units
Official record key
device-enforcement:Z-1217-2025

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 00196449015603; Lot Numbers 262560, 260893

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