# FDA recall Z-0374-2024

> **Biomet, Inc.** · Class II · device recall initiated 2023-10-09.

## Product

Compress Device Segmental Anchor Plug, 18 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement.  Item Number: 178408

## Reason for recall

Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery

## Distribution

Worldwide distribution - US Nationwide and the countries of ARGENTINA, AUSTRALIA,  CANADA, CHILE, JAPAN, NETHERLANDS, NEW ZEALAND.

## Key facts

- **Recall number:** Z-0374-2024
- **Recalling firm:** Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-10-09
- **Report date:** 2023-11-29

- **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-0374-2024

## Citation

> AI Analytics. FDA recall Z-0374-2024. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-0374-2024. Source: US FDA. Licensed CC0.

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