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 critical severity by Argus HQ. FDA published the underlying record on 2024-02-14; 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 · critical

Philips North America — Class I recall: BrightView X, gamma camera for SPECT; Model Nos.: 6-digit format 882478;…

Name: FDA Recall Record — Philips North America
Creator: Argus HQ
Published: 2024-02-14
License: https://argushq.ai/methodology

Event date: 2024-02-14 00:00:00Z
Observed: 2026-07-16 23:20:13Z
Source ID: Z-0930-2024
Payload hash: e99f838c7a12c330ebb8eeae…

Summary

Detector may unexpectedly fall due to a component failure. If the detector is positioned below center of gantry, there is a potential for abrasion, contusion, laceration, and/or fracture to the patient's lower limbs, as well as an interruption to normal system operation. If detector is positioned ab… 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 critical severity by Argus HQ. FDA published the underlying record on 2024-02-14; 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 North America — Class I recall: BrightView X, gamma camera for SPECT;    Model Nos.:    6-digit format 882478;…. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-philips-north-america-z-0930-2024

MLA

"Philips North America — Class I recall: BrightView X, gamma camera for SPECT;    Model Nos.:    6-digit format 882478;…." Argus HQ Research, Digital Empire LLC, 2024, argushq.ai/events/fda-recall-philips-north-america-z-0930-2024.

Chicago

Argus HQ Research. "Philips North America — Class I recall: BrightView X, gamma camera for SPECT;    Model Nos.:    6-digit format 882478;…." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-philips-north-america-z-0930-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_philips_north_america_z_0930_2024_2024,
  title = {Philips North America — Class I recall: BrightView X, gamma camera for SPECT;    Model Nos.:    6-digit format 882478;…},
  author = {{Argus HQ Research}},
  year = {2024},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-philips-north-america-z-0930-2024},
  note = {Accessed: July 17, 2026}
}

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