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FDA
Food and Drug Administration · Recall Z-2804-2026 · Jun 15, 2026

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

Argon Medical Devices, Inc

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. FDA Class II recall.

The remedy

Follow FDA guidance

About this recall

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

Affected identifiers

Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.

UPC 00886333210008

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Sourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.