Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505. recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIOngoing
Summary: Integra LifeSciences Corp. (NeuroSciences) is recalling Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.. Reason: Increased rate of out-of-specification endotoxin results.
What is being recalled
Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.
Why
Increased rate of out-of-specification endotoxin results.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
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 named: 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)
How to tell if yours is affected
Product ID: WSM0505. UDI-DI: 00386190001431. Lot Numbers: 7579683, 7583933, 7583891, 7583935, 7594266, 7594286, 7593011.
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-1816-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | March 19, 2026 |
| Reported | April 22, 2026 |
| Company | Integra LifeSciences Corp. (NeuroSciences) |
| Company location | Princeton, NJ, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 148 units |
More recalls from Integra LifeSciences Corp. (NeuroSciences) · all medical device recalls · recalls from March 2026