# FDA recall Z-2877-2018

> **TriMed Inc.** · Class II · device recall initiated 2018-04-16.

## Product

Ulnar Osteotomy Compression Plate, Short  Model: UOCP-S    Product Usage:  The UOCP-S is provided non-sterile with the required fixation screws and surgical instrumentation. The TriMed Ulnar Osteotomy Plate is intended for use in osteotomy procedures of the ulna.

## Reason for recall

Two instrument holes located on the side of the plate, which act to align the saw guide are located on the wrong side of the plate

## Distribution

Worldwide Distribution in the state of TX and countries of Australia, China Sweden

## Key facts

- **Recall number:** Z-2877-2018
- **Recalling firm:** TriMed Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-04-16
- **Report date:** 2018-08-29
- **Termination date:** 2021-01-28

- **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-2877-2018

## Citation

> AI Analytics. FDA recall Z-2877-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-2877-2018. Source: US FDA. Licensed CC0.

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