How many FDA warning letters has PHILIPS MEDICAL SYSTEMS received?

Argus HQ has not recorded an FDA warning letter for PHILIPS MEDICAL SYSTEMS in our current dataset.

What FDA recalls has PHILIPS MEDICAL SYSTEMS issued?

Argus HQ has recorded 1 FDA recall tied to PHILIPS MEDICAL SYSTEMS.

Is PHILIPS MEDICAL SYSTEMS FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 1 recall, and 0 approval records for PHILIPS MEDICAL SYSTEMS. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

PHILIPS MEDICAL SYSTEMS

Name: FDA Enforcement Actions Against PHILIPS MEDICAL SYSTEMS
Creator: Argus HQ
License: https://argushq.ai/methodology

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_recall2026-04-22
PHILIPS MEDICAL SYSTEMS — Class II recall: Philips Spectral CT on Rails. Model Number: 728334.

Frequently asked questions

How many FDA warning letters has PHILIPS MEDICAL SYSTEMS received?: Argus HQ has not recorded an FDA warning letter for PHILIPS MEDICAL SYSTEMS in our current dataset.
What FDA recalls has PHILIPS MEDICAL SYSTEMS issued?: Argus HQ has recorded 1 FDA recall tied to PHILIPS MEDICAL SYSTEMS.
Is PHILIPS MEDICAL SYSTEMS FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 1 recall, and 0 approval records for PHILIPS MEDICAL SYSTEMS. 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.