Juggerknot Mini Soft Anchors — Class II medical device recall Z-2619-2025
Ongoing recall by Biomet, Inc., reported 2025-10-01, distributed nationwide. The outer carton box label is for the JuggerKnot 1.0mm Mini products. However, the products within the carton
| Recall number | Z-2619-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2025-09-09 |
| Classified | 2025-09-23 |
| Reported by FDA | 2025-10-01 |
| Distributed | Nationwide (US) |
| Quantity | 40 |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00880304520950 |
| Lot numbers | 0002713620 |
| Model numbers | 912080 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2619-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.