EZDilate Wire Guided Balloon 16-17-18. Indicated for endoscopic dilation of strictures in the alimentary tract in adults and adolescents (>12 years). Model: BD-410X-1855

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UDI-DI: 00821925033269 Lot Numbers: 360769, 360770, 368258, 368259, 368844, 369417, 385724, 387425, 387426, 387794, 387795
  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:
Olympus Corporation of the Americas
Reason for Recall:
Product balloon issues: inflating, deflating and/or retrieving the devices; reports of bursting and leaking and events involving foreign body in patient and prolonged procedure.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

EZDilate Wire Guided Balloon 16-17-18. Indicated for endoscopic dilation of strictures in the alimentary tract in adults and adolescents (>12 years). Model: BD-410X-1855

Product Codes/Lot Numbers:

UDI-DI: 00821925033269 Lot Numbers: 360769, 360770, 368258, 368259, 368844, 369417, 385724, 387425, 387426, 387794, 387795

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0943-2024

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