# FDA recall Z-0314-2020

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2019-10-10.

## Product

Periarticulare Plates - Elbow, Humeral and Ulna Plates, Item Nos. 00234800504  00234800506  00234800508  00234800510  00234800512  00234800514  00234800604  00234800606  00234800608  00234800610  00234800612  00234800614  00234800712  00234800714  00234800716  00234800902  00234800904  00234800906  00234800908  00234800910  00234800912  00234800914  00234801002  00234801004  00234801006  00234801008  00234801010  00234801012

## Reason for recall

Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

## Distribution

Distributed nationwide.

## Key facts

- **Recall number:** Z-0314-2020
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-10-10
- **Report date:** 2019-11-13
- **Termination date:** 2020-05-19

- **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-0314-2020

## Citation

> AI Analytics. FDA recall Z-0314-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0314-2020. Source: US FDA. Licensed CC0.

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