# FDA recall Z-0296-2018

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2017-06-05.

## Product

Lateral Troch Plate Full Crimp - 254mm, model # 350837

## Reason for recall

Possibility that the patient label inside the product box was incorrectly labeled.  The outer box label and actual product are correctly identified but the internal patient label could be incorrect.

## Distribution

Nationwide in US; Internationally Argentina, Netherlands & Canada

## Key facts

- **Recall number:** Z-0296-2018
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-05
- **Report date:** 2018-01-10
- **Termination date:** 2018-03-06

- **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-0296-2018

## Citation

> AI Analytics. FDA recall Z-0296-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0296-2018. Source: US FDA. Licensed CC0.

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