Recall Ledger

Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710. recall (Integra LifeSciences Corp. (NeuroSciences))

Medical deviceClass IIOngoing

Summary: Integra LifeSciences Corp. (NeuroSciences) is recalling Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.. Reason: Increased rate of out-of-specification endotoxin results.

What is being recalled

Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.

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: WSM0710. UDI-DI: 00386190001448. Lot Numbers: 7579683, 7582225, 7583893, 7582227, 7583933, 7583891, 7591942, 7591944, 7583935, 7594266, 7594288, 7594286, 7593011, 7594284, 7593013.

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 numberZ-1817-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedMarch 19, 2026
ReportedApril 22, 2026
CompanyIntegra LifeSciences Corp. (NeuroSciences)
Company locationPrinceton, NJ, United States
Initiated byVoluntary: Firm initiated
Quantity46 units

More recalls from Integra LifeSciences Corp. (NeuroSciences) · all medical device recalls · recalls from March 2026

Official FDA record