How many FDA warning letters has RAYSEARCH LABORATORIES AB received?

Argus HQ has not recorded an FDA warning letter for RAYSEARCH LABORATORIES AB in our current dataset.

What FDA recalls has RAYSEARCH LABORATORIES AB issued?

Argus HQ has recorded 2 FDA recalls tied to RAYSEARCH LABORATORIES AB.

Is RAYSEARCH LABORATORIES AB FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 2 recalls, and 0 approval records for RAYSEARCH LABORATORIES AB. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

RAYSEARCH LABORATORIES AB

Name: FDA Enforcement Actions Against RAYSEARCH LABORATORIES AB
Creator: Argus HQ
License: https://argushq.ai/methodology

Industry: Medical Devices

Jurisdiction: US

FDA Warning Letter timeline

V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.

fda_recall · device_recall2026-07-08
RAYSEARCH LABORATORIES AB — Class II recall: RayCare 2024A SP4. Oncology Information Systems.
fda_recall · device_recall2026-07-08
RAYSEARCH LABORATORIES AB — Class II recall: RayCare 2024A SP1. Oncology Information Systems.

Frequently asked questions

How many FDA warning letters has RAYSEARCH LABORATORIES AB received?: Argus HQ has not recorded an FDA warning letter for RAYSEARCH LABORATORIES AB in our current dataset.
What FDA recalls has RAYSEARCH LABORATORIES AB issued?: Argus HQ has recorded 2 FDA recalls tied to RAYSEARCH LABORATORIES AB.
Is RAYSEARCH LABORATORIES AB FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 2 recalls, and 0 approval records for RAYSEARCH LABORATORIES AB. Review the linked FDA source records directly before drawing a compliance conclusion.

Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.