Has PHILIPS MEDICAL SYSTEMS had other FDA enforcement actions?

Yes. Argus HQ has recorded 11 total FDA actions tied to PHILIPS MEDICAL SYSTEMS: 0 warning letters, 11 recalls, 0 approval records, and 0 Form 483 inspection citations.

What kind of FDA record is this?

This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2026-08-05; Argus observed and indexed it on 2026-08-12.

Where can I verify this record directly with FDA?

The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

.hq

fda_recall · device_recall · high

PHILIPS MEDICAL SYSTEMS — Class II recall: Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64 Ch…

Name: FDA Recall Record — PHILIPS MEDICAL SYSTEMS
Creator: Argus HQ
Published: 2026-08-05
License: https://argushq.ai/methodology

Event date: 2026-08-05 00:00:00Z
Observed: 2026-08-12 04:20:23Z
Source ID: Z-2650-2026
Payload hash: ce52e117d2084ed3569d31eb…

Summary

The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. Additional Bolus Tracking shots may occur. This may result in the clinical acquisition being inadequate for diagnosis, causing a potential for patient rescan and receiving addition… Status: Ongoing.

Entities

PHILIPS MEDICAL SYSTEMS

View source record ↗

Frequently asked questions

Has PHILIPS MEDICAL SYSTEMS had other FDA enforcement actions?: Yes. Argus HQ has recorded 11 total FDA actions tied to PHILIPS MEDICAL SYSTEMS: 0 warning letters, 11 recalls, 0 approval records, and 0 Form 483 inspection citations.
What kind of FDA record is this?: This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2026-08-05; Argus observed and indexed it on 2026-08-12.
Where can I verify this record directly with FDA?: The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Cite this record

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

APA

Argus HQ Research (2026). PHILIPS MEDICAL SYSTEMS — Class II recall: Brilliance iCT   Brilliance iCT Upgrades  Brilliance iCT SP  Brilliance CT 64 Ch…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-philips-medical-systems-z-2650-2026

MLA

"PHILIPS MEDICAL SYSTEMS — Class II recall: Brilliance iCT   Brilliance iCT Upgrades  Brilliance iCT SP  Brilliance CT 64 Ch…." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-philips-medical-systems-z-2650-2026.

Chicago

Argus HQ Research. "PHILIPS MEDICAL SYSTEMS — Class II recall: Brilliance iCT   Brilliance iCT Upgrades  Brilliance iCT SP  Brilliance CT 64 Ch…." Digital Empire Holdings LLC. Accessed August 13, 2026. https://argushq.ai/events/fda-recall-philips-medical-systems-z-2650-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_philips_medical_systems_z_2650_2026_2026,
  title = {PHILIPS MEDICAL SYSTEMS — Class II recall: Brilliance iCT   Brilliance iCT Upgrades  Brilliance iCT SP  Brilliance CT 64 Ch…},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-philips-medical-systems-z-2650-2026},
  note = {Accessed: August 13, 2026}
}

Informational only. Not legal, financial, or medical advice.