How many FDA actions has Argon Medical Devices, Inc had?

Argus HQ has recorded 6 FDA events for Argon Medical Devices, Inc: 0 warning letters, 6 recalls, 0 approvals, and 0 Form 483 inspection observations. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

What is the most recent FDA action against Argon Medical Devices, Inc?

The most recent FDA event Argus HQ has on file for Argon Medical Devices, Inc is dated 2026-07-22, with a severity rating of "critical" in Argus HQ's classification. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

Does Argus HQ track new FDA actions for Argon Medical Devices, Inc automatically?

Yes. Argus HQ ingests FDA sources daily, including FDA warning letters, recalls, drug and biologic approvals, and Form 483 inspection observations. When a new FDA action linked to Argon Medical Devices, Inc is observed, this page's event count and history update automatically.

How many FDA actions does Argus HQ track for Argon Medical Devices, Inc?

6 total: 0 warning letters, 6 recalls, 0 approval records, and 0 Form 483 inspection citations.

Argon Medical Devices, Inc's Complete FDA Record

FDA action counts

Total FDA actions	6
Warning letters	0
Recalls	6
Approval records	0
Form 483 inspection citations	0
Most recent action	July 22, 2026

Key takeaway: Argus HQ has recorded 6 FDA events for Argon Medical Devices, Inc: 0 warning letters, 6 recalls, 0 approvals, and 0 inspection 483 observations. These events span from 2026-07-22 to 2026-07-22. The most severe rating Argus HQ has assigned across this history is "critical". Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed.

Enforcement history

On 2026-07-22, Argus HQ recorded an FDA recall for Argon Medical Devices, Inc, rated "critical" severity in Argus HQ's classification: Argon Medical Devices, Inc — Class I recall: T-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATL. On 2026-07-22, Argus HQ recorded an FDA recall for Argon Medical Devices, Inc, rated "critical" severity in Argus HQ's classification: Argon Medical Devices, Inc — Class I recall: Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F, REF: 0…. On 2026-07-22, Argus HQ recorded an FDA recall for Argon Medical Devices, Inc, rated "critical" severity in Argus HQ's classification: Argon Medical Devices, Inc — Class I recall: Bone Marrow Tray, REF: CB0033TL; CB0355TLA. On 2026-07-22, Argus HQ recorded an FDA recall for Argon Medical Devices, Inc, rated "critical" severity in Argus HQ's classification: Argon Medical Devices, Inc — Class I recall: General Biospy Tray, REF: GUTS1000. On 2026-07-22, Argus HQ recorded an FDA recall for Argon Medical Devices, Inc, rated "critical" severity in Argus HQ's classification: Argon Medical Devices, Inc — Class I recall: Arterial Line Kit 20ga x 6, REF: 400115A. On 2026-07-22, Argus HQ recorded an FDA recall for Argon Medical Devices, Inc, rated "critical" severity in Argus HQ's classification: Argon Medical Devices, Inc — Class I recall: One-Piece Introducer Tray, REF: 497455, 497434 cardiovascular. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed.

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. Argon Medical Devices, Inc has 6 separate FDA recalls on file, more than a single isolated recall event. A pattern across multiple FDA touchpoints does not by itself establish that any specific product currently poses a risk; it reflects only the frequency of FDA engagement with this company as recorded in Argus HQ's database. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ does not independently verify FDA's underlying findings; this page summarizes what FDA has published and links back to the original FDA source for each event. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

Frequently asked questions

How many FDA actions has Argon Medical Devices, Inc had?: Argus HQ has recorded 6 FDA events for Argon Medical Devices, Inc: 0 warning letters, 6 recalls, 0 approvals, and 0 Form 483 inspection observations. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.
What is the most recent FDA action against Argon Medical Devices, Inc?: The most recent FDA event Argus HQ has on file for Argon Medical Devices, Inc is dated 2026-07-22, with a severity rating of "critical" in Argus HQ's classification. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.
Does Argus HQ track new FDA actions for Argon Medical Devices, Inc automatically?: Yes. Argus HQ ingests FDA sources daily, including FDA warning letters, recalls, drug and biologic approvals, and Form 483 inspection observations. When a new FDA action linked to Argon Medical Devices, Inc is observed, this page's event count and history update automatically.
How many FDA actions does Argus HQ track for Argon Medical Devices, Inc?: 6 total: 0 warning letters, 6 recalls, 0 approval records, and 0 Form 483 inspection citations.

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

Verified from FDA.gov · Last updated: Jul 22, 2026

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's Complete FDA Record. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/company/argon-medical-devices-inc

MLA

"Argon Medical Devices, Inc's Complete FDA Record." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/company/argon-medical-devices-inc.

Chicago

Argus HQ Research. "Argon Medical Devices, Inc's Complete FDA Record." Digital Empire Holdings LLC. Accessed July 28, 2026. https://argushq.ai/company/argon-medical-devices-inc.

BibTeX

@misc{argushq_argushq_ai_company_argon_medical_devices_inc_2026,
  title = {Argon Medical Devices, Inc's Complete FDA Record},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/company/argon-medical-devices-inc},
  note = {Accessed: July 28, 2026}
}

Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗