Class II
Medical Device Recall: Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080
Biomet, Inc. · September 9, 2025
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.
States Affected
NATIONWIDE
Quantity Affected
40
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2619-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.