Class II

Medical Device Recall: Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.

Integra LifeSciences Corp. (NeuroSciences) · March 19, 2026

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.

States Affected

NATIONWIDE

Quantity Affected

148 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1816-2026

Status: ongoing

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