# FDA recall Z-1817-2026

> **Integra LifeSciences Corp. (NeuroSciences)** · Class II · device recall initiated 2026-03-19.

## Product

Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.

## Reason for recall

Increased rate of out-of-specification endotoxin results.

## Distribution

US Nationwide distribution in the states of AL, AZ, CA, DC, FL, GA, IA, IL, KS, KY, LA, MD, ME, MN, MO, MT, NC, ND, NE, NJ, NY, OH, PA, SC, SD, TN, TX, VA, VT, WA, WI, WV.

## Key facts

- **Recall number:** Z-1817-2026
- **Recalling firm:** Integra LifeSciences Corp. (NeuroSciences)
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-19
- **Report date:** 2026-04-22

- **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-1817-2026

## Citation

> AI Analytics. FDA recall Z-1817-2026. Retrieved 2026-06-04 from https://api.ai-analytics.org/recall/Z-1817-2026. Source: US FDA. Licensed CC0.

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