# FDA recall Z-0315-2020

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

## Product

PERI DIST VOLAR/DORSAL T/DORSAL DELTA RADIAL, Item Nos.   00234801303  00234801304  00234801306  00234801308  00234801310  00234801312  00234801403  00234801404  00234801406  00234801408  00234801410  00234801412  00234802102  00234802104  00234802106  00234802108  00234802110  00234802112  00234802204  00234802206  00234802208  00234802212  00234802508  00234802510  00234802608

## Reason for recall

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

## Distribution

Distributed nationwide.

## Key facts

- **Recall number:** Z-0315-2020
- **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-0315-2020

## Citation

> AI Analytics. FDA recall Z-0315-2020. Retrieved 2026-07-01 from https://api.ai-analytics.org/recall/Z-0315-2020. Source: US FDA. Licensed CC0.

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