Recall Z-2619-2025— Biomet, Inc.
Class II · Ongoing
Class II FDA medical device recall by Biomet, Inc., initiated 2025-09-09. It names one FDA 510(k) clearance: K110879. Product: Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080. Reason: 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..
- Recalling firm
- Biomet, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-09-09
- Firm location
- Warsaw, IN, United States
510(k) clearances named in this recall
1 on FDA's recordK-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.