DRAEGER, INC.
6 recall(s) on record — most severe on record: Class I.
Activity by year
- Recalls (6)
Devices registered here (1)
- Devices, Breath Trapping, AlcoholProduct code DJZ (opens in a new tab) · Class I · Clinical Toxicology · 21 CFR 862.3050
Recalls & enforcement
- Class IOngoing2026-05-07The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
- Class IOngoing2025-11-24A certain component of affected devices was not delivered within specification and contained impurities.
- Class IOngoing2025-11-10Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
- Class IOngoing2025-09-09The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
- Class IOngoing2025-06-16Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
- Class IOngoing2025-03-12The potential for cracks forming in the breathing circuit hose.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “DRAEGER, INC. (FEI 3009348423) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3009348423-draeger-inc/
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