Z-2619-2025 Class II Ongoing
FDA device recall Z-2619-2025 was initiated by Biomet, Inc. on September 9, 2025 and is designated Class II. 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. The recall status is ongoing. Affected quantity: 40.
Recall Details
- Product Type
- Devices
- Report Date
- October 1, 2025
- Initiation Date
- September 9, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 40
Product Description
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 Pattern
US Nationwide distribution.
Code Information
UDI-DI: 00880304520950; Lot Number 0002713620