# FDA recall Z-2619-2025

> **Biomet, Inc.** · Class II · device recall initiated 2025-09-09.

## Product

Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080

## Reason for recall

The outer carton box label is for the JuggerKnot 1.0mm Mini products. However, the products within the carton are JuggerKnot 1.4mm Short devices.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2619-2025
- **Recalling firm:** Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-09-09
- **Report date:** 2025-10-01

- **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-2619-2025

## Citation

> AI Analytics. FDA recall Z-2619-2025. Retrieved 2026-09-04 from https://api.ai-analytics.org/recall/Z-2619-2025. Source: US FDA. Licensed CC0.

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