FDA action counts
| Total FDA actions | 3 |
|---|---|
| Warning letters | 0 |
| Recalls | 3 |
| Approval records | 0 |
| Form 483 inspection citations | 0 |
| Most recent action | June 24, 2026 |
Risk pattern analysis
Argus HQ analysis — not an FDA finding
This section is Argus HQ analysis, not an FDA finding. Datex-Ohmeda Inc has 3 separate FDA recalls on file, more than a single isolated recall event. A pattern across multiple FDA touchpoints does not by itself establish that any specific product currently poses a risk; it reflects only the frequency of FDA engagement with this company as recorded in Argus HQ's database. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ does not independently verify FDA's underlying findings; this page summarizes what FDA has published and links back to the original FDA source for each event.
Enforcement history
On 2026-06-24, Argus HQ recorded a FDA recall for Datex-Ohmeda Inc, rated "critical" severity in Argus HQ's classification: Datex-Ohmeda Inc — Class I recall: Giraffe Stand-alone Infant Resuscitation System; Powered emergency ventilator (r… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-24, Argus HQ recorded a FDA recall for Datex-Ohmeda Inc, rated "critical" severity in Argus HQ's classification: Datex-Ohmeda Inc — Class I recall: Giraffe Warmer with Integrated Resuscitation System (iRes), Panda Warmer with In… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-24, Argus HQ recorded a FDA recall for Datex-Ohmeda Inc, rated "critical" severity in Argus HQ's classification: Datex-Ohmeda Inc — Class I recall: Panda Freestanding Warmer, Infant Radiant Warmer Product Identifiers: 2063568-00… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. In total, Datex-Ohmeda Inc has 3 FDA events on file with Argus HQ across the sources Argus HQ currently tracks (FDA Warning Letters, recalls, drug/biologic approvals, and Form 483 inspection observations). Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed.
Frequently asked questions
- What is the most recent FDA action against Datex-Ohmeda Inc?
- The most recent FDA event Argus HQ has on file for Datex-Ohmeda Inc is dated 2026-06-24, with a severity rating of "critical" in Argus HQ's classification. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.
- Does Argus HQ track new FDA actions for Datex-Ohmeda Inc automatically?
- Yes. Argus HQ ingests FDA sources daily, including FDA warning letters, recalls, drug and biologic approvals, and Form 483 inspection observations. When a new FDA action linked to Datex-Ohmeda Inc is observed, this page's event count and history update automatically.
- How many FDA actions does Argus HQ track for Datex-Ohmeda Inc?
- 3 total: 0 warning letters, 3 recalls, 0 approval records, and 0 Form 483 inspection citations.
- What is the most recent FDA action on file for Datex-Ohmeda Inc?
- June 24, 2026. Argus HQ ingests new FDA enforcement records daily.
Every FDA action tied to this company, the week it happens.
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Related enforcement actions
- Datex-Ohmeda Inc — Class I recall: Giraffe Warmer with Integrated Resuscitation System (iRes), Panda Warmer with In… →
- Datex-Ohmeda Inc — Class I recall: Giraffe Stand-alone Infant Resuscitation System; Powered emergency ventilator (r… →
- Datex-Ohmeda Inc — Class I recall: Panda Freestanding Warmer, Infant Radiant Warmer Product Identifiers: 2063568-00… →
Compare with
Two different companies merged onto this page by mistake? Or a name variant missing? Tell us — corrections@argushq.ai
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.
Argus HQ Research (2026). Datex-Ohmeda Inc — FDA Enforcement History. Digital Empire LLC. Retrieved from https://argushq.ai/company/datex-ohmeda-inc
"Datex-Ohmeda Inc — FDA Enforcement History." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/company/datex-ohmeda-inc.
Argus HQ Research. "Datex-Ohmeda Inc — FDA Enforcement History." Digital Empire LLC. Accessed July 13, 2026. https://argushq.ai/company/datex-ohmeda-inc.
@misc{argushq_argushq_ai_company_datex_ohmeda_inc_2026,
title = {Datex-Ohmeda Inc — FDA Enforcement History},
author = {{Argus HQ Research}},
year = {2026},
publisher = {Digital Empire LLC},
url = {https://argushq.ai/company/datex-ohmeda-inc},
note = {Accessed: July 13, 2026}
}Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗