Has Argon Medical Devices, Inc had other FDA enforcement actions?

Yes. Argus HQ has recorded 8 total FDA actions tied to Argon Medical Devices, Inc: 0 warning letters, 8 recalls, 0 approval records, and 0 Form 483 inspection citations.

What kind of FDA record is this?

This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2026-08-05; Argus observed and indexed it on 2026-08-12.

Where can I verify this record directly with FDA?

The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

.hq

fda_recall · device_recall · high

Argon Medical Devices, Inc — Class II recall: L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620

Name: FDA Recall Record — Argon Medical Devices, Inc
Creator: Argus HQ
Published: 2026-08-05
License: https://argushq.ai/methodology

Event date: 2026-08-05 00:00:00Z
Observed: 2026-08-12 04:20:22Z
Source ID: Z-2804-2026
Payload hash: 9b0691c8f19ff79cf0ad1ccb…

Summary

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, ther… Status: Ongoing.

Entities

Argon Medical Devices, Inc

View source record ↗

Frequently asked questions

Has Argon Medical Devices, Inc had other FDA enforcement actions?: Yes. Argus HQ has recorded 8 total FDA actions tied to Argon Medical Devices, Inc: 0 warning letters, 8 recalls, 0 approval records, and 0 Form 483 inspection citations.
What kind of FDA record is this?: This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2026-08-05; Argus observed and indexed it on 2026-08-12.
Where can I verify this record directly with FDA?: The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2026). Argon Medical Devices, Inc — Class II recall: L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-argon-medical-devices-inc-z-2804-2026

MLA

"Argon Medical Devices, Inc — Class II recall: L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-argon-medical-devices-inc-z-2804-2026.

Chicago

Argus HQ Research. "Argon Medical Devices, Inc — Class II recall: L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620." Digital Empire Holdings LLC. Accessed August 13, 2026. https://argushq.ai/events/fda-recall-argon-medical-devices-inc-z-2804-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_argon_medical_devices_inc_z_2804_2026_2026,
  title = {Argon Medical Devices, Inc — Class II recall: L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-argon-medical-devices-inc-z-2804-2026},
  note = {Accessed: August 13, 2026}
}

Informational only. Not legal, financial, or medical advice.