Argon Medical Devices, Inc: Medical Device Recall in 2022 - (Recall #: Z-0563-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: January 24, 2022

Date Posted: February 16, 2022

Recall Number: Z-0563-2022

Event ID: 89439

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.

Status: Ongoing

Product Quantity: 600 ea

Code Information:

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

Distribution Pattern:

US Nationwide distribution in the states of AL, CA, DE, IL, IN, LA, MT, NV, OH, TX, VA, TN.

Voluntary or Mandated:

Voluntary: Firm initiated