Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1215-2025 — 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

U.S. FDA — Device Enforcement · United States · 2025-01-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1215-2025
Date of alert
2025-01-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Tyber Medical
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00196449015580
Reported risk: 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
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.