# FDA recall Z-1222-2025

> **Tyber Medical** · Class II · device recall initiated 2025-01-21.

## Product

A.L.P.S. mvX-MEDIAL TIBIA PLATE 10H RT-Medial Tibia Plate, 10-Hole, Right  Intended Fixation of fractures of the distal tibia.  Model/Catalog Number: 770715102

## 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

## Distribution

Nationwide

## Key facts

- **Recall number:** Z-1222-2025
- **Recalling firm:** Tyber Medical
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-01-21
- **Report date:** 2025-03-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bethlehem, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1222-2025

## Citation

> AI Analytics. FDA recall Z-1222-2025. Retrieved 2026-07-09 from https://api.ai-analytics.org/recall/Z-1222-2025. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*