🔍 RecallPedia

Olympus Uretero-reno videoscope, Model No. URF-V2

Class I - Dangerous
🏥 Medical Devices Recalled: March 25, 2022 Olympus Corporation of the Americas Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    1 unit, serial number 2825505F UDI 04953170343582
  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:
The bending section of the URF-V2 may crack, resulting in an abnormal shape or abnormal angulation of the bending section.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Olympus Uretero-reno videoscope, Model No. URF-V2

Product Codes/Lot Numbers:

1 unit, serial number 2825505F UDI 04953170343582

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1116-2022

Related Recalls