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 high severity by Argus HQ. FDA published the underlying record on 2025-11-19; 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 Respironics, Inc. — Class II recall: SimplyGo Mini, Standard Battery Kit; Product code: 1116816; The affected bat…

Name: FDA Recall Record — Philips Respironics, Inc.
Creator: Argus HQ
Published: 2025-11-19
License: https://argushq.ai/methodology

Event date: 2025-11-19 00:00:00Z
Observed: 2026-07-16 23:20:10Z
Source ID: Z-0481-2026
Payload hash: 1a5c713e26be82efa5c0ca8b…

Summary

Certain serial numbers of the SimplyGo Mini standard battery kit contain a defective chip which can lead the battery to either fail to charge or lose voltage output when in use in the device. If the fault occurs while the device is running on battery power, the SimplyGo Mini will shut down and stop… 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 high severity by Argus HQ. FDA published the underlying record on 2025-11-19; 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 Respironics, Inc. — Class II recall: SimplyGo Mini, Standard Battery Kit;  Product code: 1116816;    The affected bat…. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-philips-respironics-inc-z-0481-2026

MLA

"Philips Respironics, Inc. — Class II recall: SimplyGo Mini, Standard Battery Kit;  Product code: 1116816;    The affected bat…." Argus HQ Research, Digital Empire LLC, 2025, argushq.ai/events/fda-recall-philips-respironics-inc-z-0481-2026.

Chicago

Argus HQ Research. "Philips Respironics, Inc. — Class II recall: SimplyGo Mini, Standard Battery Kit;  Product code: 1116816;    The affected bat…." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-philips-respironics-inc-z-0481-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_philips_respironics_inc_z_0481_2026_2025,
  title = {Philips Respironics, Inc. — Class II recall: SimplyGo Mini, Standard Battery Kit;  Product code: 1116816;    The affected bat…},
  author = {{Argus HQ Research}},
  year = {2025},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-philips-respironics-inc-z-0481-2026},
  note = {Accessed: July 17, 2026}
}

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