---
title: "L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620 — FDA record Z-2804-2026 | Is It on Recall"
description: "Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may"
url: https://isitonrecall.com/recall/fda-device-z-2804-2026-l-cath-midline-s-l-catheter-20ga-3f-1mm-x-20cm-ref-384620/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620 — FDA record Z-2804-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jun 15, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620
- **Reason**: 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.
- **Classification**: Class II
- **Recalling firm**: Argon Medical Devices, Inc
- **Quantity**: 20
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2804-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2804-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | REF/UDI-DI/Lot(Expiration): 384620/00886333210008/11490543(7/28/2026) |

Match all identifying details in the current notice. A brand name alone is not enough.

## 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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Arkansas](https://isitonrecall.com/state/arkansas/)
- [California](https://isitonrecall.com/state/california/)
- [Colorado](https://isitonrecall.com/state/colorado/)
- [Connecticut](https://isitonrecall.com/state/connecticut/)
- [Florida](https://isitonrecall.com/state/florida/)
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- [Iowa](https://isitonrecall.com/state/iowa/)
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- [Kansas](https://isitonrecall.com/state/kansas/)
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- [Maryland](https://isitonrecall.com/state/maryland/)
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- [Minnesota](https://isitonrecall.com/state/minnesota/)
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- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [North Dakota](https://isitonrecall.com/state/north-dakota/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [Nevada](https://isitonrecall.com/state/nevada/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Oregon](https://isitonrecall.com/state/oregon/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Utah](https://isitonrecall.com/state/utah/)
- [Virginia](https://isitonrecall.com/state/virginia/)
- [Washington](https://isitonrecall.com/state/washington/)

## Dates in the source

- **Report date**: Aug 5, 2026
- **Recall initiation date**: Jun 15, 2026
- **Center classification date**: Jul 24, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2804-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Argon Medical Devices, Inc records](https://isitonrecall.com/brand/argon-medical-devices-inc/)