---
title: "BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Numbe... — FDA record Z-0212-2026 | Is It on Recall"
description: "There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop"
url: https://isitonrecall.com/recall/fda-device-z-0212-2026-biomet-ziptight-acute-ac-joint-implant-single-ziploop-model-catalog-number-904834-fixation-system-fo/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834; Fixation System for AC Joint ... — FDA record Z-0212-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Sep 23, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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
- **Classification**: Class II
- **Recalling firm**: Biomet, Inc.
- **Quantity**: 98 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0212-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0212-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI-DI (01)00880304478404(17)290130(10)0002587666; Lot Number 0002587666 |

Match all identifying details in the current notice. A brand name alone is not enough.

## 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.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Oct 29, 2025
- **Recall initiation date**: Sep 23, 2025
- **Center classification date**: Oct 17, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0212-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Biomet, Inc. records](https://isitonrecall.com/brand/biomet-inc/)