Tyber Medical: Device Recall

Recall Details

Recall Number

Z-1132-2026

Classification

Class II

Product Type

Device

Recalling Firm

Tyber Medical

Status

Ongoing

Date Initiated

12/19/2025

Location

Bethlehem, PA, United States

Voluntary/Mandated

Voluntary: Firm initiated

Product Quantity

64 units

Reason for Recall

The supplier manufactured anatomical left plates with an incorrect thread orientation.

Product Description

Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate 6Hd/14Shaft/Left/Std/186mm Model/Catalog Number: 02.426.691S Product Description: 2 Column Distal Radius Plate - 6 Head, 14 Shaft, Standard Left - 186mm Component: No

Distribution Pattern

US Nationwide distribution in the state of PA.

Other Recalls by Tyber Medical

• Class II: Risk 12/19/2025
  The supplier manufactured anatomical left plates with an incorrect thread orientation.
• Class II: Risk 01/21/2025
  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
• Class II: Risk 01/21/2025
  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
• Class II: Risk 01/21/2025
  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
• Class II: Risk 01/21/2025
  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

View all recalls by Tyber Medical →