FDAFDA · Food and drugs·Recall number Z-2804-2026
L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620
Published August 5, 2026 · Recall initiated: June 15, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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 to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Argon Medical Devices, Inc
- Distributor
- 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
- Lot
- REF/UDI-DI/Lot(Expiration): 384620/00886333210008/11490543(7/28/2026)
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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