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
- Recalling Firm
- Argon Medical Devices, Inc
- 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.
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