Has Philips North America had other FDA enforcement actions?

Yes. Argus HQ has recorded 355 total FDA actions tied to Philips North America: 0 warning letters, 355 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 2023-11-22; Argus observed and indexed it on 2026-07-16.

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 North America Llc — Class II recall: Brilliance CT Big Bore with software version V4.8.0.10421 Model:728244 CT sc…

Name: FDA Recall Record — Philips North America
Creator: Argus HQ
Published: 2023-11-22
License: https://argushq.ai/methodology

Event date: 2023-11-22 00:00:00Z
Observed: 2026-07-16 23:20:13Z
Source ID: Z-0293-2024
Payload hash: 327a88ffbe21b1e4f3be5b51…

Summary

For oncology users: If the user performed off-set reconstruction on CT device a shift could be observed on the contouring area of the primary and secondary images sets when using image fusion (on TPS) and incorrect coordinates may be sent to TPS system when using absolute patient marking. This may l… Status: Ongoing.

Entities

Philips North America

View source record ↗

Frequently asked questions

Has Philips North America had other FDA enforcement actions?: Yes. Argus HQ has recorded 355 total FDA actions tied to Philips North America: 0 warning letters, 355 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 2023-11-22; Argus observed and indexed it on 2026-07-16.
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 (2023). Philips North America Llc — Class II recall: Brilliance CT Big Bore with software version V4.8.0.10421  Model:728244    CT sc…. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-philips-north-america-llc-z-0293-2024

MLA

"Philips North America Llc — Class II recall: Brilliance CT Big Bore with software version V4.8.0.10421  Model:728244    CT sc…." Argus HQ Research, Digital Empire LLC, 2023, argushq.ai/events/fda-recall-philips-north-america-llc-z-0293-2024.

Chicago

Argus HQ Research. "Philips North America Llc — Class II recall: Brilliance CT Big Bore with software version V4.8.0.10421  Model:728244    CT sc…." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-philips-north-america-llc-z-0293-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_philips_north_america_llc_z_0293_2024_2023,
  title = {Philips North America Llc — Class II recall: Brilliance CT Big Bore with software version V4.8.0.10421  Model:728244    CT sc…},
  author = {{Argus HQ Research}},
  year = {2023},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-philips-north-america-llc-z-0293-2024},
  note = {Accessed: July 17, 2026}
}

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