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Serious recall: Injury is possible or has been reported. Take action promptly.

Integra LifeSciences Corp. (NeuroSciences) 2026-04-22 Health serious FDA
Health · FDA · Recall #FDA-Z-1820-2026

Cytal Burn Matrix 10x15 cm. Product ID: BMM1015. Recall

Issued April 22, 2026 · Integra LifeSciences Corp. (NeuroSciences)

In April 2026, Integra LifeSciences Corp. (NeuroSciences) recalled the Cytal Burn Matrix 10x15 cm. Product ID: BMM1015., a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Increased rate of out-of-specification endotoxin results.

What you should do

  1. 1 Stop using Cytal Burn Matrix 10x15 cm. Product ID: BMM1015. right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Integra LifeSciences Corp. (NeuroSciences) to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Integra LifeSciences Corp. (NeuroSciences)
Category
Health
Recall date
April 22, 2026
Units affected
Not reported
Sold at
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,
Recall number
FDA-Z-1820-2026
Made in
United States
Issuing agency
FDA

In context

Read the official FDA notice

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