Medical device recalls Moderate risk

Integra LifeSciences Corp. (NeuroSciences) recalls Cytal Burn Matrix 7x10 cm. Product ID: BMM0710.

Recall date
March 19, 2026
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1819-2026
FDA classification
Class II
Brand / firm
Integra LifeSciences Corp. (NeuroSciences)
Sold / distributed
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.

Why it was recalled

Increased rate of out-of-specification endotoxin results.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Cytal Burn Matrix 7x10 cm. Product ID: BMM0710.

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