# FDA recall Z-0057-2021

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2020-08-14.

## Product

Dual Mobility Vivacit-E Bearing, Model Number 110031009

## Reason for recall

The outer package is labeled as a Size C 38 mm, however, the implant inside the package is a Size E 42 mm.

## Distribution

Products were distributed to the following US states: FL, ID, IL, IN, KY, MA, MD, MI, MN, NC, NJ, OH, OR, PA, SC, TX, UT, VA, WI, and WV.

## Key facts

- **Recall number:** Z-0057-2021
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-08-14
- **Report date:** 2020-10-14
- **Termination date:** 2022-06-09

- **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-0057-2021

## Citation

> AI Analytics. FDA recall Z-0057-2021. Retrieved 2026-08-12 from https://api.ai-analytics.org/recall/Z-0057-2021. Source: US FDA. Licensed CC0.

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