Biomet, Inc. recalls BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Mo
See all recalls from Biomet, Inc. →Recalled Product
BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834; Fixation System for AC Joint Repair
Hazard / Issue
There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop
Issued by
FDA
Distribution: 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.
Lot/Code Info: UDI-DI (01)00880304478404(17)290130(10)0002587666; Lot Number 0002587666
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for BIOMET ZipTight, Acute AC →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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