# FDA recall Z-1284-2023

> **Biomet, Inc.** · Class II · device recall initiated 2023-02-06.

## Product

G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462

## Reason for recall

The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner.

## Distribution

US Distribution to states of:  AZ, FL, GA, MI, NE, and TX.

## Key facts

- **Recall number:** Z-1284-2023
- **Recalling firm:** Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-02-06
- **Report date:** 2023-03-29

- **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-1284-2023

## Citation

> AI Analytics. FDA recall Z-1284-2023. Retrieved 2026-07-05 from https://api.ai-analytics.org/recall/Z-1284-2023. Source: US FDA. Licensed CC0.

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