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FDA (Device enforcement)Recalled 2026-06-15class ii

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

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.

Details from the source

Reason for recall: 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. Distribution: 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 Quantity: 20 Lot/code info: REF/UDI-DI/Lot(Expiration): 384620/00886333210008/11490543(7/28/2026)

UPC codes

00886333210008

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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