TemporaryFDAOngoing
Can cause harm that is usually temporary.
L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620
Check the device or its packaging for
REF/UDI-DI/Lot(Expiration): 384620/00886333210008/11490543(7/28/2026)
- Why
- 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.
- Distributed
- 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
- Company
- Argon Medical Devices, Inc
- Announced
- This is the date the recall was announced. A company may have started it weeks earlier.
- Recall began
Source: FDA record Z-2804-2026 · retrieved 24 July 2026
Read the official notice