FDA action counts
| Total FDA actions | 2 |
|---|---|
| Warning letters | 0 |
| Recalls | 2 |
| Approval records | 0 |
| Form 483 inspection citations | 0 |
| Most recent action | July 8, 2026 |
Enforcement history
On 2026-07-08, Argus HQ recorded an FDA recall for Hamilton Medical AG, rated "high" severity in Argus HQ's classification: Hamilton Medical AG — Class II recall: IntelliCuff, Portable automatic cuff pressure controller REF: 951001. On 2026-07-08, Argus HQ recorded an FDA recall for Hamilton Medical AG, rated "critical" severity in Argus HQ's classification: Hamilton Medical AG — Class I recall: Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HA…. 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. 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. Hamilton Medical AG has 2 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
- What is the most recent FDA action against Hamilton Medical AG?
- The most recent FDA event Argus HQ has on file for Hamilton Medical AG is dated 2026-07-08, 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 Hamilton Medical AG 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 Hamilton Medical AG is observed, this page's event count and history update automatically.
- How many FDA actions does Argus HQ track for Hamilton Medical AG?
- 2 total: 0 warning letters, 2 recalls, 0 approval records, and 0 Form 483 inspection citations.
- What is the most recent FDA action on file for Hamilton Medical AG?
- July 8, 2026. Argus HQ ingests new FDA enforcement records daily.
Every FDA action tied to this company, the week it happens.
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Related enforcement actions
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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 8, 2026Cite this record
Reusing this data in reporting or research? Here’s a ready-made citation.
Argus HQ Research (2026). FDA Enforcement History: Hamilton Medical AG. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/company/hamilton-medical-ag
"FDA Enforcement History: Hamilton Medical AG." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/company/hamilton-medical-ag.
Argus HQ Research. "FDA Enforcement History: Hamilton Medical AG." Digital Empire Holdings LLC. Accessed August 29, 2026. https://argushq.ai/company/hamilton-medical-ag.
@misc{argushq_argushq_ai_company_hamilton_medical_ag_2026,
title = {FDA Enforcement History: Hamilton Medical AG},
author = {{Argus HQ Research}},
year = {2026},
publisher = {Digital Empire Holdings LLC},
url = {https://argushq.ai/company/hamilton-medical-ag},
note = {Accessed: August 29, 2026}
}Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗

