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

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.

On 6/15/2026, recall notices were emailed to customers who were asked to do the following: 1) Provide this recall notice to all people who need to be aware within your organization or to any organization where the potentially affected product has been transferred. 2) Segregate, quarantine, and return affected devices to recalling firm. 3) Complete and return the response form via email Arbee.cummings@argonmedical.com For additional information on this letter, please email Scott.Bishop@argonmedical.com

• FDA enforcement recordOfficial FDA database entry for Z-2804-2026
• FDA 510(k) clearance · K230669The device's official FDA premarket clearance record
• FDA device classification · LJSOfficial FDA classification for this device type
• CFR regulation · 21 CFR 880.5970The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find Argon Medical Devices, IncSearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.