FDA Device recall Z-0212-2026
BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834
- FDA Device
- Class II
- ongoing
- Published 2025-10-29
On 2025-10-29 the FDA classified a Class II recall of BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834 by Biomet, citing there is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0212-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-09-23 |
| Published | 2025-10-29 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Biomet |
| Distribution | n/a |
Product
BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834; Fixation System for AC Joint Repair
Reason
There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop
Identifiers
| code_info | UDI-DI (01)00880304478404(17)290130(10)0002587666; Lot Number 0002587666 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0212-2026%22
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