Does Argus HQ track new FDA actions for Maquet Cardiovascular, LLC 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 Maquet Cardiovascular, LLC is observed, this page's event count and history update automatically.

How many FDA actions does Argus HQ track for Maquet Cardiovascular, LLC?

1 total: 0 warning letters, 1 recall, 0 approval records, and 0 Form 483 inspection citations.

What is the most recent FDA action on file for Maquet Cardiovascular, LLC?

July 22, 2026. Argus HQ ingests new FDA enforcement records daily.

Has Maquet Cardiovascular, LLC had product recalls?

Yes, 1 recall on file. See the full history below for each one.

Maquet Cardiovascular, LLC — FDA Compliance Timeline

At a glance: Argus HQ has recorded 1 FDA events for Maquet Cardiovascular, LLC: 0 warning letters, 1 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 "high". 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.

FDA action counts

Total FDA actions	1
Warning letters	0
Recalls	1
Approval records	0
Form 483 inspection citations	0
Most recent action	July 22, 2026

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. Maquet Cardiovascular, LLC has 1 FDA event on file. 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.

Enforcement history

On 2026-07-22, Argus HQ recorded an FDA recall for Maquet Cardiovascular, LLC, rated "high" severity in Argus HQ's classification: Maquet Cardiovascular, LLC — Class II recall: The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI…. 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.

Frequently asked questions

Does Argus HQ track new FDA actions for Maquet Cardiovascular, LLC 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 Maquet Cardiovascular, LLC is observed, this page's event count and history update automatically.
How many FDA actions does Argus HQ track for Maquet Cardiovascular, LLC?: 1 total: 0 warning letters, 1 recall, 0 approval records, and 0 Form 483 inspection citations.
What is the most recent FDA action on file for Maquet Cardiovascular, LLC?: July 22, 2026. Argus HQ ingests new FDA enforcement records daily.
Has Maquet Cardiovascular, LLC had product recalls?: Yes, 1 recall on file. See the full history below for each one.

Every FDA action tied to this company, the week it happens.

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Maquet Cardiovascular, LLC — Class II recall: The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI… →

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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). Maquet Cardiovascular, LLC — FDA Compliance Timeline. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/company/maquet-cardiovascular-llc

MLA

"Maquet Cardiovascular, LLC — FDA Compliance Timeline." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/company/maquet-cardiovascular-llc.

Chicago

Argus HQ Research. "Maquet Cardiovascular, LLC — FDA Compliance Timeline." Digital Empire Holdings LLC. Accessed July 28, 2026. https://argushq.ai/company/maquet-cardiovascular-llc.

BibTeX

@misc{argushq_argushq_ai_company_maquet_cardiovascular_llc_2026,
  title = {Maquet Cardiovascular, LLC — FDA Compliance Timeline},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/company/maquet-cardiovascular-llc},
  note = {Accessed: July 28, 2026}
}

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