company
Draeger, 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_recall2026-06-10Draeger, Inc. — Class I recall: Atlan A350. Model Number: 8211500. anesthesia workstation
- fda_recall · device_recall2026-06-10Draeger, Inc. — Class I recall: Atlan A350XL. Model Number: 8621600. anesthesia workstation
Frequently asked questions
- How many FDA warning letters has Draeger, Inc. received?
- Argus HQ has not recorded an FDA warning letter for Draeger, Inc. in our current dataset.
- What FDA recalls has Draeger, Inc. issued?
- Argus HQ has recorded 2 FDA recalls tied to Draeger, Inc..
- Is Draeger, Inc. FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 2 recalls, and 0 approval records for Draeger, 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.

