FDA recall Z-2619-2025

Biomet, Inc. · Class II · device

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

Status
Ongoing
Initiation date
2025-09-09
Report date
2025-10-01
Voluntary/Mandated
Voluntary: Firm initiated
Location
Warsaw, IN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2619-2025