company
Datex-Ohmeda Inc
Jurisdiction: US
FDA Warning Letter timeline
V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.
- fda_recall · device_recall2026-06-24Datex-Ohmeda Inc — Class I recall: Giraffe Warmer with Integrated Resuscitation System (iRes), Panda Warmer with In…
- fda_recall · device_recall2026-06-24Datex-Ohmeda Inc — Class I recall: Giraffe Stand-alone Infant Resuscitation System; Powered emergency ventilator (r…
- fda_recall · device_recall2026-06-24Datex-Ohmeda Inc — Class I recall: Panda Freestanding Warmer, Infant Radiant Warmer Product Identifiers: 2063568-00…
Frequently asked questions
- How many FDA warning letters has Datex-Ohmeda Inc received?
- Argus HQ has not recorded an FDA warning letter for Datex-Ohmeda Inc in our current dataset.
- What FDA recalls has Datex-Ohmeda Inc issued?
- Argus HQ has recorded 3 FDA recalls tied to Datex-Ohmeda Inc.
- Is Datex-Ohmeda Inc FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 3 recalls, and 0 approval records for Datex-Ohmeda Inc. Review the linked FDA source records directly before drawing a compliance conclusion.
Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.