Recall
FDAHealthJune 15, 2026

Argon Medical Devices, Inc — L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620

⚠️ 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.

Is this relevant to me?

Geography
US, AR, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, MA, MD, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OR, TN, TX, UT, VA, WA
Source agency
FDA
Category
Health
Published
June 15, 2026

US: AR, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, MA, MD, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OR, TN, TX, UT, VA, WA. OUS: MYS, CAN, SAU

What's affected?

Product
L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620
Lot code
(Expiration):

Additional details

REF/UDI-DI/Lot(Expiration): 384620/00886333210008/11490543(7/28/2026)

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 20.

View original FDA notice →

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