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 2023-12-20; 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 Llc — Class I recall: Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 7813…

Name: FDA Recall Record — Philips North America
Creator: Argus HQ
Published: 2023-12-20
License: https://argushq.ai/methodology

Event date: 2023-12-20 00:00:00Z
Observed: 2026-07-16 23:20:13Z
Source ID: Z-0505-2024
Payload hash: eabd7f7884b67aefe10cbfce…

Summary

Firm was informed of an event in which the structural integrity of the MR system components failed due to unintended excessive pressure buildup of helium gas during a magnet quench. If the system is unable to contain the pressured helium gas due to an unforeseen blockage in the system, risks to pati… 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 2023-12-20; 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 North America Llc — Class I recall: Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 7813…. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-philips-north-america-llc-z-0505-2024

MLA

"Philips North America Llc — Class I recall: Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 7813…." Argus HQ Research, Digital Empire LLC, 2023, argushq.ai/events/fda-recall-philips-north-america-llc-z-0505-2024.

Chicago

Argus HQ Research. "Philips North America Llc — Class I recall: Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 7813…." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-philips-north-america-llc-z-0505-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_philips_north_america_llc_z_0505_2024_2023,
  title = {Philips North America Llc — Class I recall: Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 7813…},
  author = {{Argus HQ Research}},
  year = {2023},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-philips-north-america-llc-z-0505-2024},
  note = {Accessed: July 17, 2026}
}

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