Integra Lifesciences Corp. (neurosciences): Cytal Wound Matrix 2-layer 7x10 Cm. Product Id: Wsm0710
Recall Summary Integra LifeSciences is recalling Cytal Wound Matrix 2-Layer 7x10 cm (product ID: WSM0710), a wound care device distributed nationwide, because some units have higher-than-acceptable levels of endotoxin, a bacterial substance that can cause immune reactions. This is a Class II recall, meaning the product could cause serious health problems but is unlikely to cause death. The affected product was distributed across the United States.
- Recalling firm
- Integra LifeSciences Corp. (NeuroSciences)
- Product
- Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.
- Reason
- Increased rate of out-of-specification endotoxin results.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-03-19
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- 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.
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/bc972c17-6812-4bb7-805f-3670d444ee0e