HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 8mmx8mm UPN: M00553530

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    GTIN: 08714729904557 Lot Numbers: 33335139, 33335340, 33336413, 33511491, 34015885, 34065661, 34068983, 34101926
  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:
Boston Scientific Corporation
Reason for Recall:
Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 8mmx8mm UPN: M00553530

Product Codes/Lot Numbers:

GTIN: 08714729904557 Lot Numbers: 33335139, 33335340, 33336413, 33511491, 34015885, 34065661, 34068983, 34101926

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1033-2025

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