1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6"

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    1. Model: 400115A and Serial # 11377499, Expire Date: 10/27/2022 2. Model: 498100 and Serial # 11378381, Expire Date: 4/15/2026
  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:
Argon Medical Devices, Inc
Reason for Recall:
Guidewire included with two lots of Arterial Line Kits would not fit through the needle of the same kit. This could potentially lead to a slight delay in the procedure and minor blood loss.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6"

Product Codes/Lot Numbers:

1. Model: 400115A and Serial # 11377499, Expire Date: 10/27/2022 2. Model: 498100 and Serial # 11378381, Expire Date: 4/15/2026

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0563-2022

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