# FDA recall Z-0305-2020

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

## Product

ZPLP Fibular Plate, Item Nos. 00234701504  00234701506  00234701508  00234701510  00234701512  00234701516  00234701604  00234701606  00234701608  00234701610  00234701612  00234701614  00234701616  00234701702  00234701704  00234701706  00234701708  00234701710  00234701712  00234701714  00234701716  00234701718  00234701802  00234701804  00234701806  00234701808  00234701810  00234701812  00234701814  00234701816  00234701818  47235701704  47235701706  47235701708  47235701710  47235701712  47235701714  47235701716  47235701804  47235701806  47235701808  47235701810  47235701812  47235701814  47235701816

## Reason for recall

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

## Distribution

Distributed nationwide.

## Key facts

- **Recall number:** Z-0305-2020
- **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-0305-2020

## Citation

> AI Analytics. FDA recall Z-0305-2020. Retrieved 2026-07-17 from https://api.ai-analytics.org/recall/Z-0305-2020. Source: US FDA. Licensed CC0.

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