# FDA recall Z-0932-2024

> **TriMed Inc.** · Class II · device recall initiated 2023-11-28.

## Product

Volar Bearing Plate.     REF: VBEAL-3-7N, VBEAL-5-7N, VBEAL-3-7S, VBEAL-5-7S, VBEAL-7-7S, VBEAL-3-7W, VBEAL-5-7W, VBEAR-3-7N, VBEAR-5-7-N, VBEAR-3-7S, VBEAR-5-7S, VBEAR-7-7S, VBEAR-3-7W, VBEAR-5-7W.    Intended to be used as an aid to the treatment of certain types of fractures, non-unions or osteotomies.

## Reason for recall

Plates, part of a wrist fixation system, are affixed during surgery with bearings that may pop out from distal peg holes.

## Distribution

US: FL, MI, AL, NY, CA

## Key facts

- **Recall number:** Z-0932-2024
- **Recalling firm:** TriMed Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-11-28
- **Report date:** 2024-02-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Santa Clarita, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0932-2024

## Citation

> AI Analytics. FDA recall Z-0932-2024. Retrieved 2026-07-17 from https://api.ai-analytics.org/recall/Z-0932-2024. Source: US FDA. Licensed CC0.

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