Argon Medical Devices recalls two lots of arterial line kits where the guidewire might not fit through the needle, potentially causing minor delays and blood loss during procedures.
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.
Argon Medical Devices is recalling two specific models of arterial line kits because the included guidewire may not fit through the needle. This could cause minor delays and small blood loss during medical procedures.
The guidewire included with the kits may not fit through the needle, which could cause a slight delay in the procedure and minor blood loss. This issue is specific to the two recalled lots and does not involve serious injury risks.
Healthcare professionals using these arterial line kits for procedures are most at risk. Patients receiving these kits during medical procedures may experience minor delays or small blood loss.
Check for model numbers 400115A (serial # 11377499, expires 10/27/2022) or 498100 (serial # 11378381, expires 4/15/2026). These kits were sold with specific expiration dates.
Identify the model number and serial number to confirm if your kit is in the recalled lots.
The guidewire included with these kits may not fit through the needle, potentially causing minor delays and small blood loss during procedures.
Check for model numbers 400115A (serial # 11377499, expires 10/27/2022) or 498100 (serial # 11378381, expires 4/15/2026).
The recall does not specify a remedy, so contact Argon Medical Devices for further instructions.
We’ve drafted a message you can send Argon Medical Devices to request your refund or repair — edit it as you like.
Subject: Recall Z-0563-2022 — Argon Medical Devices Argon Medical Devices Hello, I own a Argon Medical Devices that is covered by recall Z-0563-2022 from Argon Medical Devices. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
