# FDA recall Z-2556-2025

> **Omnia Medical** · Class II · device recall initiated 2024-07-15.

## Product

TiBrid Stand Alone Intervertebral Body Fusion Device, SA Angled Punch Awl, Sizes: 30 degree, 45 degree and 60 degree.

## Reason for recall

Failure of fusion system instruments in the field.

## Distribution

US Nationwide distribution in the states of AZ, CA, NJ, NV, OK & WA.

## Key facts

- **Recall number:** Z-2556-2025
- **Recalling firm:** Omnia Medical
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-07-15
- **Report date:** 2025-09-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Morgantown, WV, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2556-2025

## Citation

> AI Analytics. FDA recall Z-2556-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2556-2025. Source: US FDA. Licensed CC0.

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