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 medium severity by Argus HQ. FDA published the underlying record on 2025-09-03; 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 · medium

Philips Ultrasound, Inc — Class III recall: S4-2 Transducer Probe

Name: FDA Recall Record — Philips Ultrasound, Inc
Creator: Argus HQ
Published: 2025-09-03
License: https://argushq.ai/methodology

Event date: 2025-09-03 00:00:00Z
Observed: 2026-07-16 23:20:10Z
Source ID: Z-2393-2025
Payload hash: 48c962f767da0775349e9356…

Summary

To provide clarification and labelling to define the useful life of ultrasound transducers in the field. Status: Ongoing.

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 medium severity by Argus HQ. FDA published the underlying record on 2025-09-03; 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 (2025). Philips Ultrasound, Inc — Class III recall: S4-2 Transducer Probe. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-philips-ultrasound-inc-z-2393-2025

MLA

"Philips Ultrasound, Inc — Class III recall: S4-2 Transducer Probe." Argus HQ Research, Digital Empire LLC, 2025, argushq.ai/events/fda-recall-philips-ultrasound-inc-z-2393-2025.

Chicago

Argus HQ Research. "Philips Ultrasound, Inc — Class III recall: S4-2 Transducer Probe." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-philips-ultrasound-inc-z-2393-2025.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_philips_ultrasound_inc_z_2393_2025_2025,
  title = {Philips Ultrasound, Inc — Class III recall: S4-2 Transducer Probe},
  author = {{Argus HQ Research}},
  year = {2025},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-philips-ultrasound-inc-z-2393-2025},
  note = {Accessed: July 17, 2026}
}

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