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FDA · Medical devices ·

L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm recall

Argon Medical Devices, Inc recalled L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm on August 5, 2026 because of 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. It was sold in 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.

Why it was recalled

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.

What's recalled

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

Quantity: 20

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Argon Medical Devices, Inc, Athens, TX
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
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
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
Status
Ongoing
Recall number
Z-2804-2026
Source
U.S. Food and Drug Administration

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