Has Philips Respironics, Inc. had other FDA enforcement actions?

Yes. Argus HQ has recorded 50 total FDA actions tied to Philips Respironics, Inc.: 0 warning letters, 50 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 2023-01-18; 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 Respironics, Inc. — Class I recall: Philips Garbin Ventilator, Model Number 1058180B

Name: FDA Recall Record — Philips Respironics, Inc.
Creator: Argus HQ
Published: 2023-01-18
License: https://argushq.ai/methodology

Event date: 2023-01-18 00:00:00Z
Observed: 2026-07-16 23:20:13Z
Source ID: Z-0884-2023
Payload hash: e829d0b55b0013e308923117…

Summary

The replacement silicone sound abatement foam installed into some Trilogy 100 and Trilogy 200 devices may separate from the plastic backing to which it is attached. If this were to happen, the foam could potentially block air inlet, which could result in a reduction in delivered therapy volume or pr… Status: Ongoing.

Entities

Philips Respironics, Inc.

View source record ↗

Frequently asked questions

Has Philips Respironics, Inc. had other FDA enforcement actions?: Yes. Argus HQ has recorded 50 total FDA actions tied to Philips Respironics, Inc.: 0 warning letters, 50 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 2023-01-18; 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 Respironics, Inc. — Class I recall: Philips Garbin Ventilator, Model Number 1058180B. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-philips-respironics-inc-z-0884-2023

MLA

"Philips Respironics, Inc. — Class I recall: Philips Garbin Ventilator, Model Number 1058180B." Argus HQ Research, Digital Empire LLC, 2023, argushq.ai/events/fda-recall-philips-respironics-inc-z-0884-2023.

Chicago

Argus HQ Research. "Philips Respironics, Inc. — Class I recall: Philips Garbin Ventilator, Model Number 1058180B." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-philips-respironics-inc-z-0884-2023.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_philips_respironics_inc_z_0884_2023_2023,
  title = {Philips Respironics, Inc. — Class I recall: Philips Garbin Ventilator, Model Number 1058180B},
  author = {{Argus HQ Research}},
  year = {2023},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-philips-respironics-inc-z-0884-2023},
  note = {Accessed: July 17, 2026}
}

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