L-Cath Midline S/L Catheter 20ga — Class II medical device recall Z-2804-2026
Ongoing recall by Argon Medical Devices, Inc, reported 2026-08-05, distributed in AR, CA, CO, CT, FL, GA, IA, ID…. Catheters, indicated for short/long-term peripheral access to central venous system for the administration of
| Recall number | Z-2804-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Argon Medical Devices, Inc, Athens, TX, United States |
| Recall initiated | 2026-06-15 |
| Classified | 2026-07-24 |
| Reported by FDA | 2026-08-05 |
| Distributed | 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 |
| Quantity | 20 |
| Reason classes | packaging, device malfunction |
| UPC / GTIN / UDI-DI | 00886333210008 |
| Model numbers | 384620 |
Product
L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2804-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.