PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: February 16, 2022 Initiated: January 24, 2022 #Z-0563-2022

Product Description

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

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.

Details

Units Affected
600 ea
Distribution
US Nationwide distribution in the states of AL, CA, DE, IL, IN, LA, MT, NV, OH, TX, VA, TN.
Location
Athens, TX

Frequently Asked Questions

What product was recalled?
1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6". Recalled by Argon Medical Devices, Inc. Units affected: 600 ea.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 16, 2022. Severity: Moderate. Recall number: Z-0563-2022.