Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    LOT: 051724B/ UDI: B006LTE7003PS52
  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:
Neurovision Medical Products Inc
Reason for Recall:
mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO

Product Codes/Lot Numbers:

LOT: 051724B/ UDI: B006LTE7003PS52

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2719-2024

Related Recalls

Product packaging contains the wrong part number and kit contents.

May 19, 2025 Surgical Instruments View Details →

The electrode insulating material on the Cobra EMG ET tube used for continuous EMG monitoring may soften over time so that it may be more susceptible to damage by scratching or bending, which could stop or inhibit the EMG signal transmission of the electrodes to the monitor and render the device not usable.

Jul 21, 2020 Diagnostic Equipment Nationwide View Details →

The electrode insulating material on the Cobra EMG ET tube used for continuous EMG monitoring may soften over time so that it may be more susceptible to damage by scratching or bending, which could stop or inhibit the EMG signal transmission of the electrodes to the monitor and render the device not usable.

Jul 21, 2020 Diagnostic Equipment Nationwide View Details →