🔍 RecallPedia

eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156

Class I - Dangerous
🏥 Medical Devices Recalled: March 2, 2026 Civco Medical Instruments Co. Surgical Instruments

What Should You Do?

  1. Check if you have this product:
    UDI-DI: 00841436111072; Lot Number: A276634
  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 was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156

Product Codes/Lot Numbers:

UDI-DI: 00841436111072; Lot Number: A276634

Distribution:

Distributed in: US, OH, PA, WA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1735-2026

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