🔍 RecallPedia

RadiaLux Lighted Retractor (Pink), REF: 50-101-1

Class I - Dangerous
🏥 Medical Devices Recalled: December 8, 2022 Medtronic Navigation Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI-DI/Lot: 00763000432805/ 705F, 706F, 707F, 708F, 709F
  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:
Medtronic Navigation, Inc.
Reason for Recall:
Defect in sterile pouch seal, incomplete seal, of lighted Retractors, increases the risk of contamination, which can lead to post-operative infection.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

RadiaLux Lighted Retractor (Pink), REF: 50-101-1

Product Codes/Lot Numbers:

UDI-DI/Lot: 00763000432805/ 705F, 706F, 707F, 708F, 709F

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0953-2023

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