Reported Feb 16, 2022 · Ongoing
1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6"
Argon Medical Devices, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Argon Medical Devices, Inc · 1445 Flat Creek Rd · Athens, TX · 75751-5002
Is this the product you have?
- 1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6"
- Lot codes and dates
- 1
- Model400115A and Serial # 11377499
- Expire Date10/27/2022 2
- Model498100 and Serial # 11378381
- Expire Date4/15/2026
- Amount recalled
- 600 ea
Where it was sold
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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