Argon Medical Devices recalls L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm (REF 384620) due to hub leaks and cracks causing infection risks. Affected patients should contact for remedy.
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or cracking at the hub, which may lead to replacement, inability to flush/aspirate catheter, catheter occlusion, therapy interruption, blood loss, tissue irritation, bloodstream infection.
Argon Medical Devices is recalling a specific type of midline catheter because it can leak or crack at the hub, leading to infections or treatment interruptions. This affects patients using the catheter for medical treatments.
The catheter's hub can leak or crack, which may cause the catheter to become blocked, stop working properly, or lead to infections. This happens during normal medical use and can interrupt treatments.
Patients using the L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm (REF 384620) for medical treatments are affected. Those with the catheter in place are most at risk.
Check for the model: L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm with reference number 384620. The product was sold with expiration date 7/28/2026.
Identify the reference number 384620 on the catheter packaging or label.
The recall indicates potential hub leaks and cracks that could cause infections or treatment interruptions, so it is not safe to use without remedy.
The recall record does not specify a remedy or replacement process.
The catheter was sold with an expiration date of 7/28/2026.
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-2804-2026 — Argon Medical Devices Argon Medical Devices Hello, I own a Argon Medical Devices that is covered by recall Z-2804-2026 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.
