Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin); BOX LOBECTOMIA VATS 3D; CFN: BOX06170V4;

Class I - Dangerous
🏥 Medical Devices Recalled: September 25, 2025 Covidien Diagnostic Equipment Nationwide

What Should You Do?

  1. Check if you have this product:
    CFN: BOX06170V4; UDI-DI: 00763000988975; Lot numbers: 0231961695;
  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:
Covidien, LP
Reason for Recall:
A manufacturing issue could lead to a malformed cover tube press which can lead to internal components' movement during firing - leading to the potential for uncontrolled motion.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin); BOX LOBECTOMIA VATS 3D; CFN: BOX06170V4;

Product Codes/Lot Numbers:

CFN: BOX06170V4; UDI-DI: 00763000988975; Lot numbers: 0231961695;

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0486-2026

Related Recalls

Due to customer complaint regarding incorrect display box labeling.

Apr 15, 2026 Other Medical Devices Nationwide View Details →

Due to complaints and investigations stating that alarms from the primary patient bedside monitor was not alarming/being transmitted and received on the remote patient monitoring system.

Jan 30, 2026 Diagnostic Equipment Nationwide View Details →