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FDA (Device enforcement)Recalled 2025-09-23class ii

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

Hazard

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

Details from the source

Reason for recall: There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop 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. Quantity: 98 units Lot/code info: UDI-DI (01)00880304478404(17)290130(10)0002587666; Lot Number 0002587666

UPC codes

00880304478404

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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