HomeMedical Device recalls
High severity

Draeger Vapor 3000. Unheated, calibrated anesthetic vaporizer.

SourceFDA Device Enforcement
CategoryMedical Device
SeverityHigh
Statusongoing
Recall dateNovember 24, 2025
ReportedDecember 31, 2025
Recalling firmDraeger, Inc.
Country / regionUnited States PA

Hazard

A certain component of affected devices was not delivered within specification and contained impurities.

Affected products

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