---
title: "L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x ... — FDA record Z-2638-2024 | Is It on Recall"
description: "Peripherally Inserted Central Catheter (PICC) is labeled 26G/1.9Fr x 30cm but package contains incorrect 26G/1.9Fr x 50cm PICC, which could lead to procedural d"
url: https://isitonrecall.com/recall/fda-device-z-2638-2024-l-cath-picc-s-l-peripherally-inserted-central-catheter-26ga-1-9f-0-60mm-x-30cm-ref-384539/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 384539 — FDA record Z-2638-2024

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 14, 2024. 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 PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 384539
- **Reason**: Peripherally Inserted Central Catheter (PICC) is labeled 26G/1.9Fr x 30cm but package contains incorrect 26G/1.9Fr x 50cm PICC, which could lead to procedural delay.
- **Classification**: Class II
- **Recalling firm**: Argon Medical Devices, Inc
- **Quantity**: 155
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2638-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2638-2024%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 | UDI-DI: 20886333209938, 00886333209934. Lot: 11563923. Expiration: 2027-03-11 |

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

## Distribution

US distribution to the states of: TX, WA, CA, IL

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

- [California](https://isitonrecall.com/state/california/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Washington](https://isitonrecall.com/state/washington/)

## Dates in the source

- **Report date**: Aug 21, 2024
- **Recall initiation date**: Jun 14, 2024
- **Center classification date**: Aug 15, 2024

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-2638-2024%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/)