Reported Aug 5, 2026 · Ongoing

L-Cath PICC S/L Peripherally Inserted Central Catheter

Argon Medical Devices, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Argon Medical Devices, Inc · 1445 Flat Creek Rd · Athens, TX · 75751-5002

Is this the product you have?

L-Cath PICC S/L Peripherally Inserted Central Catheter

4 products · 19 lot codes

  1. 38453918ga (3.5F) 1.15mm x 60cm

    UDI-DI
    00886333209934

    7 recalled lot codes

    • 114881677/14/2026
    • 114881687/17/2026
    • 11494535E8/1/2026
    • 1150776611/13/2026
    • 1155078012/12/2026
    • 1155148712/15/2026
    • 1155148812/15/2026
  2. 384464Basic Kit 28GA (1.2F) x 25cm 1 Lumen)

    UDI-DI
    00886333209835

    2 recalled lot codes

    • 114905937/28/2026
    • 11494886(8/28/2026)1150115010/6/2026
  3. 38451620ga (3F) 1.00mm x 60cm

    UDI-DI
    00886333209910

    8 recalled lot codes

    • 115004108/14/2026
    • 115018568/14/2026
    • 115042229/9/2026
    • 115069529/9/2026
    • 115238689/18/2026
    • 115517899/18/2026
    • 1155390911/13/2026
    • 1155922611/20/2026
  4. 384463

    UDI-DI
    00886333209828

    2 recalled lot codes

    • 114907978/1/2026
    • 114909598/11/2026
Amount recalled
6928

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Argon Medical Devices, Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 2:52 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.