Notice names this product. Argon Medical Devices’s L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm is named in FDA Class II recall Z-2804-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported 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. Identifying details: REF/UDI-DI/Lot(Expiration): 384620/00886333210008/11490543(7/28/2026). Units affected: 20. Status: Ongoing.
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking a…
Company / brand: Argon Medical Devices
Affected product: L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm
Official ID Z-2804-2026 · Official record ↗
See all Argon Medical Devices recalls →
Found something wrong or missing? Report a data error.
Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.