# FDA recall Z-0477-2025

> **Biomet, Inc.** · Class II · device recall initiated 2024-10-21.

## Product

JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357

## Reason for recall

Firm received complaints reporting that guides were warped when pulled out of packaging. This issue may result in extension of surgery to find another product, or may lead to adverse local tissue reaction leading to surgical intervention.

## Distribution

Worldwide distribution - US Nationwide and the countries of Australia, Brazil, Canada, Singapore, Switzerland.

## Key facts

- **Recall number:** Z-0477-2025
- **Recalling firm:** Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-10-21
- **Report date:** 2024-11-27

- **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-0477-2025

## Citation

> AI Analytics. FDA recall Z-0477-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0477-2025. Source: US FDA. Licensed CC0.

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