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 2024-05-15; 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: 5000 Compact Series Ultrasound Systems, Product/REF: 5500 CV/795141, 5500 P/7951…

Name: FDA Recall Record — Philips Ultrasound, Inc
Creator: Argus HQ
Published: 2024-05-15
License: https://argushq.ai/methodology

Event date: 2024-05-15 00:00:00Z
Observed: 2026-07-16 23:20:11Z
Source ID: Z-1757-2024
Payload hash: a4251e7695d375b0c062ffc0…

Summary

Ultrasound system with: 1) transesophageal echocardiography transducer (TEE) connected/not selected 2) 1, 2 non-TEE connected 3) Imaging with non-TEE 4) Selected/not selected imaging transducer removed 5) Transducer connected 6) Non-TEE imaging continues, Then though TEE is unselected, it may have p… 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 high severity by Argus HQ. FDA published the underlying record on 2024-05-15; 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 (2024). Philips Ultrasound, Inc. — Class II recall: 5000 Compact Series Ultrasound Systems, Product/REF: 5500 CV/795141, 5500 P/7951…. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-philips-ultrasound-inc-z-1757-2024

MLA

"Philips Ultrasound, Inc. — Class II recall: 5000 Compact Series Ultrasound Systems, Product/REF: 5500 CV/795141, 5500 P/7951…." Argus HQ Research, Digital Empire LLC, 2024, argushq.ai/events/fda-recall-philips-ultrasound-inc-z-1757-2024.

Chicago

Argus HQ Research. "Philips Ultrasound, Inc. — Class II recall: 5000 Compact Series Ultrasound Systems, Product/REF: 5500 CV/795141, 5500 P/7951…." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-philips-ultrasound-inc-z-1757-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_philips_ultrasound_inc_z_1757_2024_2024,
  title = {Philips Ultrasound, Inc. — Class II recall: 5000 Compact Series Ultrasound Systems, Product/REF: 5500 CV/795141, 5500 P/7951…},
  author = {{Argus HQ Research}},
  year = {2024},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-philips-ultrasound-inc-z-1757-2024},
  note = {Accessed: July 17, 2026}
}

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