United StatesBIOMET ZipTight Acute AC Joint Implant, Single Ziploop (Model/Catalog Number 904834; Lot Number 0002587666; UDI-DI (01)00880304478404(17)290130(10)0002587666) is being recalled. The lot was recalled because there is a potential for a missing slotted button assembly in that lot.
What's being recalled
BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834; Fixation System for AC Joint Repair
Recalling firm: Biomet, Inc., Warsaw, IN, United States.
How to identify it
UDI-DI (01)00880304478404(17)290130(10)0002587666; Lot Number 0002587666
The hazard
There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
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.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)