# FDA recall Z-0626-2018

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2017-08-25.

## Product

G7 DUAL MOBILITY LINER 44MM F    Product Usage:  Intended for use in hip arthroplasty cases which involves the removal of the damaged joint and tissues to be replaced with artificial prosthesis. The result of the procedure is to relieve pain and restore a sense of normal function and mobility to the damaged joint.

## Reason for recall

The affected products are labeled and etched as F-44 mm liners; however, the physical products could potentially be E-42 mm liners.

## Distribution

US Nationwide Distribution

## Key facts

- **Recall number:** Z-0626-2018
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-08-25
- **Report date:** 2018-02-21
- **Termination date:** 2018-08-16

- **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-0626-2018

## Citation

> AI Analytics. FDA recall Z-0626-2018. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0626-2018. Source: US FDA. Licensed CC0.

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