Biomet, Inc.: Medical Device Recall in 2025 - (Recall #: Z-2619-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080

Product Classification:

Class II

Date Initiated: September 9, 2025

Date Posted: October 1, 2025

Recall Number: Z-2619-2025

Event ID: 97570

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.

Status: Ongoing

Product Quantity: 40

Code Information:

UDI-DI: 00880304520950; Lot Number 0002713620

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated