🔍 RecallPedia

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

Class I - Dangerous
🏥 Medical Devices Recalled: January 21, 2025 Tyber Medical Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI-DI; 00196449015528 Lot Numbers 24043BU03, 267844, 24043BU02, 261286
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Tyber Medical
Reason for Recall:
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
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

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

Product Codes/Lot Numbers:

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

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1209-2025

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