Biomet, Inc.: Device Recall

Recall #Z-2619-2025 · 09/09/2025

Class II: Risk

Recall Details

Recall Number: Z-2619-2025
Classification: Class II
Product Type: Device
Recalling Firm: Biomet, Inc.
Status: Ongoing
Date Initiated: 09/09/2025
Location: Warsaw, IN, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 40

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.

Product Description

Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080

Distribution Pattern

US Nationwide distribution.

Other Recalls by Biomet, Inc.

Class II: Risk 09/23/2025

There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop
Class II: Risk 10/21/2024

Firm received complaints reporting that guides were warped when pulled out of packaging. This issue may result in extension of surgery to find another product, or may lead to adverse local tissue reaction leading to surgical intervention.
Class II: Risk 05/17/2024

41 mm acetabular outer heads were potentially assembled with a 42 mm locking ring, may lead to joint instability leading requiring surgical intervention

View all recalls by Biomet, Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.