🔍 RecallPedia

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

Class I - Dangerous
🏥 Medical Devices Recalled: March 19, 2026 Integra LifeSciences Corp. (NeuroSciences) Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Product ID: BMM1015. UDI-DI: 00386190001110. Lot Numbers: 7579681, 7582225, 7582227, 7583933, 7591942, 7591944, 7583935, 7593018, 7594284, 7593013.
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Integra LifeSciences Corp. (NeuroSciences)
Reason for Recall:
Increased rate of out-of-specification endotoxin results.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

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

Product Codes/Lot Numbers:

Product ID: BMM1015. UDI-DI: 00386190001110. Lot Numbers: 7579681, 7582225, 7582227, 7583933, 7591942, 7591944, 7583935, 7593018, 7594284, 7593013.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1820-2026

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