Has PHILIPS MEDICAL SYSTEMS had other FDA enforcement actions?

Yes. Argus HQ has recorded 8 total FDA actions tied to PHILIPS MEDICAL SYSTEMS: 0 warning letters, 8 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 2024-02-21; 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 MEDICAL SYSTEMS — Class II recall: CombiDiagnost R90 1.0 (709030)

Name: FDA Recall Record — PHILIPS MEDICAL SYSTEMS
Creator: Argus HQ
Published: 2024-02-21
License: https://argushq.ai/methodology

Event date: 2024-02-21 00:00:00Z
Observed: 2026-07-16 23:20:13Z
Source ID: Z-1087-2024
Payload hash: 33c126313cf1ef212600f172…

Summary

While performing a fluoroscopy examination, there is a potential that the Radio Fluoroscopy (RF) viewer will also display a previous patient's radiography images. If the issue occurs, there will be differences in image content, image format and image size. 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 8 total FDA actions tied to PHILIPS MEDICAL SYSTEMS: 0 warning letters, 8 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 2024-02-21; 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 (2024). PHILIPS MEDICAL SYSTEMS — Class II recall: CombiDiagnost R90 1.0 (709030). Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-philips-medical-systems-z-1087-2024

MLA

"PHILIPS MEDICAL SYSTEMS — Class II recall: CombiDiagnost R90 1.0 (709030)." Argus HQ Research, Digital Empire LLC, 2024, argushq.ai/events/fda-recall-philips-medical-systems-z-1087-2024.

Chicago

Argus HQ Research. "PHILIPS MEDICAL SYSTEMS — Class II recall: CombiDiagnost R90 1.0 (709030)." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-philips-medical-systems-z-1087-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_philips_medical_systems_z_1087_2024_2024,
  title = {PHILIPS MEDICAL SYSTEMS — Class II recall: CombiDiagnost R90 1.0 (709030)},
  author = {{Argus HQ Research}},
  year = {2024},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-philips-medical-systems-z-1087-2024},
  note = {Accessed: July 17, 2026}
}

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