🔍 RecallPedia

IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System. Indicated for palliative treatment of biliary strictures produced by malignant neoplasms

Class I - Dangerous
🏥 Medical Devices Recalled: May 29, 2012 IDEV Technologies Implants & Prosthetics Nationwide

What Should You Do?

  1. Check if you have this product:
    Model Number: S-05-100-120-G3; Lot Number 01049037
  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:
IDEV Technologies, Inc.
Reason for Recall:
There was an error on the outer labeling of this device. The inner label was correct.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System. Indicated for palliative treatment of biliary strictures produced by malignant neoplasms

Product Codes/Lot Numbers:

Model Number: S-05-100-120-G3; Lot Number 01049037

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1550-2013