🔍 RecallPedia

Artelon FlexBand Plus Ref: 41054 & 41057

Class I - Dangerous
🏥 Medical Devices Recalled: February 6, 2026 International Life Sciences Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    REF: 41054 -Lot: A10010201/GTIN: 00850003396064 REF: 41057 - Lot: A10010101/GTIN: 00850003396033
  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:
International Life Sciences
Reason for Recall:
Augmentation devices failed bacterial endotoxin testing.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Artelon FlexBand Plus Ref: 41054 & 41057

Product Codes/Lot Numbers:

REF: 41054 -Lot: A10010201/GTIN: 00850003396064 REF: 41057 - Lot: A10010101/GTIN: 00850003396033

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1555-2026

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