Argon Medical Devices, Inc 2022-02-16 Health serious FDA
Health · FDA · Recall #FDA-Z-0563-2022
1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6" Recall
Issued February 16, 2022 · Argon Medical Devices, Inc
In February 2022, Argon Medical Devices, Inc recalled the 1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6", a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using 1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6" right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Argon Medical Devices, Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Argon Medical Devices, Inc
- Category
- Health
- Recall date
- February 16, 2022
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the states of AL, CA, DE, IL, IN, LA, MT, NV, OH, TX, VA, TN.
- Recall number
- FDA-Z-0563-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- Argon Medical Devices, Inc has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.