# FDA recall Z-0514-2020

> **Howmedica Osteonics Corp.** · Class II · device recall initiated 2019-10-03.

## Product

Stryker X-Change Medial Wall Mesh Small (6-Petal)-Intended to be implanted to replace a hip joint  REF 0942-8-025

## Reason for recall

Boxes of the 6-Petal X-Change Wall Mesh Small (Part # 0942-8-025) contain the 4-Petal X-Change Wall Mesh Small (Part # 0942-8-015)

## Distribution

Foreign: Australia, France, Finland, Germany, Italy, Japan, New Zealand, Netherlands, Norway, Romania, Spain, Sweden and UK

## Key facts

- **Recall number:** Z-0514-2020
- **Recalling firm:** Howmedica Osteonics Corp.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-10-03
- **Report date:** 2019-12-04
- **Termination date:** 2022-04-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mahwah, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0514-2020

## Citation

> AI Analytics. FDA recall Z-0514-2020. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-0514-2020. Source: US FDA. Licensed CC0.

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