What is the most recent FDA action against RAYSEARCH LABORATORIES AB?

The most recent FDA event Argus HQ has on file for RAYSEARCH LABORATORIES AB 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 RAYSEARCH LABORATORIES AB 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 RAYSEARCH LABORATORIES AB is observed, this page's event count and history update automatically.

How many FDA actions does Argus HQ track for RAYSEARCH LABORATORIES AB?

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 RAYSEARCH LABORATORIES AB?

July 8, 2026. Argus HQ ingests new FDA enforcement records daily.

Regulatory Record: RAYSEARCH LABORATORIES AB

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

In short: Argus HQ has recorded 2 FDA events for RAYSEARCH LABORATORIES AB: 0 warning letters, 2 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. RAYSEARCH LABORATORIES AB 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.

Enforcement history

On 2026-07-08, Argus HQ recorded an FDA recall for RAYSEARCH LABORATORIES AB, rated "high" severity in Argus HQ's classification: RAYSEARCH LABORATORIES AB — Class II recall: RayCare 2024A SP1. Oncology Information Systems.. On 2026-07-08, Argus HQ recorded an FDA recall for RAYSEARCH LABORATORIES AB, rated "high" severity in Argus HQ's classification: RAYSEARCH LABORATORIES AB — Class II recall: RayCare 2024A SP4. Oncology Information Systems.. 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

What is the most recent FDA action against RAYSEARCH LABORATORIES AB?: The most recent FDA event Argus HQ has on file for RAYSEARCH LABORATORIES AB 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 RAYSEARCH LABORATORIES AB 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 RAYSEARCH LABORATORIES AB is observed, this page's event count and history update automatically.
How many FDA actions does Argus HQ track for RAYSEARCH LABORATORIES AB?: 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 RAYSEARCH LABORATORIES AB?: July 8, 2026. Argus HQ ingests new FDA enforcement records daily.

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

Free weekly briefing. Real-time alerts on paid plans.

Compare with

Two different companies merged onto this page by mistake? Or a name variant missing? Tell us — corrections@argushq.ai

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). Regulatory Record: RAYSEARCH LABORATORIES AB. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/company/raysearch-laboratories-ab

MLA

"Regulatory Record: RAYSEARCH LABORATORIES AB." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/company/raysearch-laboratories-ab.

Chicago

Argus HQ Research. "Regulatory Record: RAYSEARCH LABORATORIES AB." Digital Empire Holdings LLC. Accessed August 29, 2026. https://argushq.ai/company/raysearch-laboratories-ab.

BibTeX

@misc{argushq_argushq_ai_company_raysearch_laboratories_ab_2026,
  title = {Regulatory Record: RAYSEARCH LABORATORIES AB},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/company/raysearch-laboratories-ab},
  note = {Accessed: August 29, 2026}
}

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