Has Philips Ultrasound, Inc had other FDA enforcement actions?

Yes. Argus HQ has recorded 105 total FDA actions tied to Philips Ultrasound, Inc: 0 warning letters, 105 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 2023-11-15; 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 Ultrasound, Inc. — Class II recall: Philips EPIQ Diagnostic Ultrasound System Models: EPIQ 7G(model # 795200), EPIQ…

Name: FDA Recall Record — Philips Ultrasound, Inc
Creator: Argus HQ
Published: 2023-11-15
License: https://argushq.ai/methodology

Event date: 2023-11-15 00:00:00Z
Observed: 2026-07-16 23:20:13Z
Source ID: Z-0283-2024
Payload hash: 8b2f6f960a29fb6f40f33520…

Summary

Their is the potential that diagnostic ultrasound systems operating with software version 10.0 may present a delayed image instead of a real time image. Status: Completed.

Entities

Philips Ultrasound, Inc

View source record ↗

Frequently asked questions

Has Philips Ultrasound, Inc had other FDA enforcement actions?: Yes. Argus HQ has recorded 105 total FDA actions tied to Philips Ultrasound, Inc: 0 warning letters, 105 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 2023-11-15; 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 Ultrasound, Inc. — Class II recall: Philips EPIQ Diagnostic Ultrasound System Models:  EPIQ 7G(model # 795200), EPIQ…. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-philips-ultrasound-inc-z-0283-2024

MLA

"Philips Ultrasound, Inc. — Class II recall: Philips EPIQ Diagnostic Ultrasound System Models:  EPIQ 7G(model # 795200), EPIQ…." Argus HQ Research, Digital Empire LLC, 2023, argushq.ai/events/fda-recall-philips-ultrasound-inc-z-0283-2024.

Chicago

Argus HQ Research. "Philips Ultrasound, Inc. — Class II recall: Philips EPIQ Diagnostic Ultrasound System Models:  EPIQ 7G(model # 795200), EPIQ…." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-philips-ultrasound-inc-z-0283-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_philips_ultrasound_inc_z_0283_2024_2023,
  title = {Philips Ultrasound, Inc. — Class II recall: Philips EPIQ Diagnostic Ultrasound System Models:  EPIQ 7G(model # 795200), EPIQ…},
  author = {{Argus HQ Research}},
  year = {2023},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-philips-ultrasound-inc-z-0283-2024},
  note = {Accessed: July 17, 2026}
}

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