# FDA recall Z-2638-2024

> **Argon Medical Devices, Inc** · Class II · device recall initiated 2024-06-14.

## Product

L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 384539

## Reason for recall

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.

## Distribution

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

## Key facts

- **Recall number:** Z-2638-2024
- **Recalling firm:** Argon Medical Devices, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-14
- **Report date:** 2024-08-21

- **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-2638-2024

## Citation

> AI Analytics. FDA recall Z-2638-2024. Retrieved 2026-08-17 from https://api.ai-analytics.org/recall/Z-2638-2024. Source: US FDA. Licensed CC0.

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