FDA Medical devices recall ·
Cytal Wound Matrix 2-Layer 10x15 cm recall
- Recall number
- Z-1818-2026
- Date
- (initiated March 19, 2026)
- Company / brand
- Integra LifeSciences Corp. (NeuroSciences)
1100 Campus Rd, Princeton, NJ, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 452 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.
Why was it recalled?
Increased rate of out-of-specification endotoxin results.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Product ID: WSM1015. UDI-DI: 00386190001455. Lot Numbers: 7579681, 7582225, 7583893, 7582227, 7591942, 7591944, 7583935, 7594266, 7593018, 7594288, 7594284, 7593013.
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: Alabama Arizona California District of Columbia Florida Georgia Iowa Illinois Kansas Kentucky Louisiana Maryland Maine Minnesota Missouri Montana North Carolina North Dakota Nebraska New Jersey New York Ohio Pennsylvania South Carolina South Dakota Tennessee Texas Virginia Vermont Washington Wisconsin West Virginia
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1818-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.