Is this FDA enforcement data for Laborie Medical Technologies Corp official?

Every record links directly to its primary FDA.gov source. Argus HQ aggregates and structures public FDA data; the verbatim FDA record is always the source of truth.

How many FDA actions has Laborie Medical Technologies Corp had?

Argus HQ has recorded 1 FDA events for Laborie Medical Technologies Corp: 0 warning letters, 1 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 Laborie Medical Technologies Corp?

The most recent FDA event Argus HQ has on file for Laborie Medical Technologies Corp is dated 2026-07-08, with a severity rating of "high" 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 Laborie Medical Technologies Corp 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 Laborie Medical Technologies Corp is observed, this page's event count and history update automatically.

Laborie Medical Technologies Corp — FDA Enforcement History

FDA action counts

Total FDA actions	1
Warning letters	0
Recalls	1
Approval records	0
Form 483 inspection citations	0
Most recent action	July 8, 2026

The short version: Argus HQ has recorded 1 FDA events for Laborie Medical Technologies Corp: 0 warning letters, 1 recalls, 0 approvals, and 0 inspection 483 observations. These events span from 2026-07-08 to 2026-07-08. 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.

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. Laborie Medical Technologies Corp 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 2026-07-08, Argus HQ recorded an FDA recall for Laborie Medical Technologies Corp, rated "high" severity in Argus HQ's classification: Laborie Medical Technologies Corp — Class II recall: Solar GI System (Water Perfusion); Product Name (Catalog Number): Solar GI LGI…. 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

Is this FDA enforcement data for Laborie Medical Technologies Corp official?: Every record links directly to its primary FDA.gov source. Argus HQ aggregates and structures public FDA data; the verbatim FDA record is always the source of truth.
How many FDA actions has Laborie Medical Technologies Corp had?: Argus HQ has recorded 1 FDA events for Laborie Medical Technologies Corp: 0 warning letters, 1 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 Laborie Medical Technologies Corp?: The most recent FDA event Argus HQ has on file for Laborie Medical Technologies Corp is dated 2026-07-08, with a severity rating of "high" 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 Laborie Medical Technologies Corp 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 Laborie Medical Technologies Corp is observed, this page's event count and history update automatically.

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Laborie Medical Technologies Corp — Class II recall: Solar GI System (Water Perfusion); Product Name (Catalog Number): Solar GI LGI… →

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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, 2026

Cite this record

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

APA

Argus HQ Research (2026). Laborie Medical Technologies Corp — FDA Enforcement History. Digital Empire LLC. Retrieved from https://argushq.ai/company/laborie-medical-technologies-corp

MLA

"Laborie Medical Technologies Corp — FDA Enforcement History." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/company/laborie-medical-technologies-corp.

Chicago

Argus HQ Research. "Laborie Medical Technologies Corp — FDA Enforcement History." Digital Empire LLC. Accessed July 15, 2026. https://argushq.ai/company/laborie-medical-technologies-corp.

BibTeX

@misc{argushq_argushq_ai_company_laborie_medical_technologies_corp_2026,
  title = {Laborie Medical Technologies Corp — FDA Enforcement History},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/company/laborie-medical-technologies-corp},
  note = {Accessed: July 15, 2026}
}

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