Biomet, Inc.: Medical Device Recall in 2025 - (Recall #: Z-0212-2026)

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:

BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834; Fixation System for AC Joint Repair

Product Classification:

Class II

Date Initiated: September 23, 2025

Date Posted: October 29, 2025

Recall Number: Z-0212-2026

Event ID: 97670

Reason for Recall:

There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop

Status: Ongoing

Product Quantity: 98 units

Code Information:

UDI-DI (01)00880304478404(17)290130(10)0002587666; Lot Number 0002587666

Distribution Pattern:

Refer to the attached ZFA 2025-00166_Initial Consignee List and ZFA 2025-00166_Initial Distribution History containing the distribution and the identification of the domestic consignees.

Voluntary or Mandated:

Voluntary: Firm initiated