Has Datex-Ohmeda Inc had other FDA enforcement actions?

Yes. Argus HQ has recorded 7 total FDA actions tied to Datex-Ohmeda Inc: 0 warning letters, 7 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 2026-09-23; Argus observed and indexed it on 2026-09-29.

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

Datex-Ohmeda, Inc. — Class II recall: Aisys, Datex-Ohmeda anesthesia system, Part Number 1011-9050-000

Name: FDA Recall Record — Datex-Ohmeda Inc
Creator: Argus HQ
Published: 2026-09-23
License: https://argushq.ai/methodology

Event date: 2026-09-23 00:00:00Z
Observed: 2026-09-29 04:20:37Z
Source ID: Z-3189-2026
Payload hash: 863fdb468e06494480144cf4…

Summary

Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 100% O2 to the breathing system enabling continued controlled or manual ventilation and initiates audible and visual alarm… Status: Ongoing.

Entities

Datex-Ohmeda Inc

View source record ↗

Frequently asked questions

Has Datex-Ohmeda Inc had other FDA enforcement actions?: Yes. Argus HQ has recorded 7 total FDA actions tied to Datex-Ohmeda Inc: 0 warning letters, 7 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 2026-09-23; Argus observed and indexed it on 2026-09-29.
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 (2026). Datex-Ohmeda, Inc. — Class II recall: Aisys, Datex-Ohmeda anesthesia system, Part Number 1011-9050-000. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-datex-ohmeda-inc-z-3189-2026

MLA

"Datex-Ohmeda, Inc. — Class II recall: Aisys, Datex-Ohmeda anesthesia system, Part Number 1011-9050-000." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-datex-ohmeda-inc-z-3189-2026.

Chicago

Argus HQ Research. "Datex-Ohmeda, Inc. — Class II recall: Aisys, Datex-Ohmeda anesthesia system, Part Number 1011-9050-000." Digital Empire Holdings LLC. Accessed September 29, 2026. https://argushq.ai/events/fda-recall-datex-ohmeda-inc-z-3189-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_datex_ohmeda_inc_z_3189_2026_2026,
  title = {Datex-Ohmeda, Inc. — Class II recall: Aisys, Datex-Ohmeda anesthesia system, Part Number 1011-9050-000},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-datex-ohmeda-inc-z-3189-2026},
  note = {Accessed: September 29, 2026}
}

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