# FDA recall Z-0906-2022

> **Integra LifeSciences Corp.** · Class II · device recall initiated 2022-02-28.

## Product

Integra Universal Flexible Arm part number REF 1362275

## Reason for recall

Excess force used to tighten the Universal Flexible Arm can cause the internal cable to break at the tip, resulting in an unusable condition.

## Distribution

US Nationwide Distribution: AL, AZ, FL, GA, IL, MA, MD, NY, OH, OR, PA, TX

## Key facts

- **Recall number:** Z-0906-2022
- **Recalling firm:** Integra LifeSciences Corp.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-02-28
- **Report date:** 2022-04-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Princeton, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0906-2022

## Citation

> AI Analytics. FDA recall Z-0906-2022. Retrieved 2026-08-12 from https://api.ai-analytics.org/recall/Z-0906-2022. Source: US FDA. Licensed CC0.

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