🔍 RecallPedia

VirtuTRAX Instrument Navigator, Sensor with 10 17 GA VirtutTRAX

Class I - Dangerous
🏥 Medical Devices Recalled: October 8, 2021 Civco Medical Instruments Co. Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    Part Number 610-1080; UDI 00841436101936; Lot Numbers: A109102, A109175, A121363, A129087, A129088, A131042, A133436, A134220, A138099, A139369, A140674, A141818
  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:
Civco Medical Instruments Co. Inc.
Reason for Recall:
There is potential that the VirtuTRAX device will not tighten onto the instrument to be used.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

VirtuTRAX Instrument Navigator, Sensor with 10 17 GA VirtutTRAX

Product Codes/Lot Numbers:

Part Number 610-1080; UDI 00841436101936; Lot Numbers: A109102, A109175, A121363, A129087, A129088, A131042, A133436, A134220, A138099, A139369, A140674, A141818

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0397-2022

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