# FDA recall Z-0939-2018

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2018-01-03.

## Product

Trabecular Metal¿ Primary Hip Prosthesis; Part Numbers: 1. 00-7864-013-00 (UDI: (01) 00889024139251 (17) 250731 (10) 63703649), and 2. 00-7864-013-20 (UDI: (01) 00889024139268 (17) 250731 (10) 63703681)

## Reason for recall

Two lots of hip implants are  mislabeled.

## Distribution

Distributed in 2  US states: LA and NY. Distributed in Canada, China, Japan, and Switzerland.

## Key facts

- **Recall number:** Z-0939-2018
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-01-03
- **Report date:** 2018-03-21
- **Termination date:** 2019-04-11

- **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-0939-2018

## Citation

> AI Analytics. FDA recall Z-0939-2018. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0939-2018. Source: US FDA. Licensed CC0.

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