Cytal Wound Matrix 2-Layer 10x15 cm. Product ID recall: Endotoxin
Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.
Why was Cytal Wound Matrix 2-Layer 10x15 cm. Product ID recalled?
Increased rate of out-of-specification endotoxin results.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Product ID: WSM1015. UDI-DI: 00386190001455. Lot Numbers: 7579681, 7582225, 7583893, 7582227, 7591942, 7591944, 7583935, 7594266, 7593018, 7594288, 7594284, 7593013.
- Product
- Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.
- Recalling firm
- Integra LifeSciences Corp. (NeuroSciences)
- Quantity
- 452 units
- 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.
- Recall date
- April 22, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)