# FDA recall Z-0212-2026

> **Biomet, Inc.** · Class II · device recall initiated 2025-09-23.

## Product

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

## 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.

## Key facts

- **Recall number:** Z-0212-2026
- **Recalling firm:** Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-09-23
- **Report date:** 2025-10-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Warsaw, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0212-2026

## Citation

> AI Analytics. FDA recall Z-0212-2026. Retrieved 2026-09-21 from https://api.ai-analytics.org/recall/Z-0212-2026. Source: US FDA. Licensed CC0.

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