🔍 RecallPedia

Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.

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: WSM0505. UDI-DI: 00386190001431. Lot Numbers: 7579683, 7583933, 7583891, 7583935, 7594266, 7594286, 7593011.
  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 Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.

Product Codes/Lot Numbers:

Product ID: WSM0505. UDI-DI: 00386190001431. Lot Numbers: 7579683, 7583933, 7583891, 7583935, 7594266, 7594286, 7593011.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1816-2026

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