🔍 RecallPedia

Bander Ureteral Diversion Open-End Stent Set, Global Product No. G14822 G14823

Class I - Dangerous
🏥 Medical Devices Recalled: January 4, 2019 Cook Implants & Prosthetics Nationwide

What Should You Do?

  1. Check if you have this product:
    8011030 8033568 8063430 8063431 8150491 8417631 8417632 8587162 8587163 8590532 8590533 7990830 8003084 8033571 8063428 8590520 8590522 8629475 NS8629473
  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:
Cook Inc.
Reason for Recall:
The wire guide may be incorrectly loaded into the wire guide holder, leading to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Bander Ureteral Diversion Open-End Stent Set, Global Product No. G14822 G14823

Product Codes/Lot Numbers:

8011030 8033568 8063430 8063431 8150491 8417631 8417632 8587162 8587163 8590532 8590533 7990830 8003084 8033571 8063428 8590520 8590522 8629475 NS8629473

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0972-2020

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