# FDA recall Z-2804-2026

> **Argon Medical Devices, Inc** · Class II · device recall initiated 2026-06-15.

## 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.

## 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

## Key facts

- **Recall number:** Z-2804-2026
- **Recalling firm:** Argon Medical Devices, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-06-15
- **Report date:** 2026-08-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Athens, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2804-2026

## Citation

> AI Analytics. FDA recall Z-2804-2026. Retrieved 2026-09-02 from https://api.ai-analytics.org/recall/Z-2804-2026. Source: US FDA. Licensed CC0.

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