# FDA recall Z-2965-2018

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2018-07-12.

## Product

Peg Fully Threaded, Locking, 2.5mm x 10mm, Item Number 131212610 Orthopedic device used for stabilization and fixation of small bone fragments     Intended for stabilization and fixation of small bone fragments in fresh fractures, revision procedures, joint fusion and reconstructions of small bones of the hand, foot, wrist, ankle, humerus, scapula, finger, toe, pelvis and craniomaxillofacial skeleton, particularly in osteopenic bone.

## Reason for recall

A size 22mm threaded peg was found in the package of a 10mm unit.

## Distribution

International Distribution to countries of: Japan and Netherlands.

## Key facts

- **Recall number:** Z-2965-2018
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-07-12
- **Report date:** 2018-09-12
- **Termination date:** 2020-05-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Warsaw, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2965-2018

## Citation

> AI Analytics. FDA recall Z-2965-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-2965-2018. Source: US FDA. Licensed CC0.

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