Medical Device Recall: Draeger Vapor 3000. Unheated, calibrated anesthetic vaporizer.
Draeger, Inc. · November 24, 2025
Reason for Recall
A certain component of affected devices was not delivered within specification and contained impurities.
Distribution
Worldwide - US Nationwide distribution in the states of AK, CA, FL, IA, KS, MD, ME, MN, NY, OH, PA, RI, SD, TN, TX, UT, W and the countries of Argentina, Australia, Belgium, Brazil, Cambodia, China, Columbia, Czech Republic, Ecuador, Egypt, France, Germany, Greece, Guatemala, Hungary, Indonesia, Israel, Japan, Kenya, Mexico, Nepal, Norway, Panama, Peru, Philippines, Poland, Romania, Saudi Arabia, Serbia, Singapore, Spain, Thailand, Turkey, United Kingdom, United Arab Emirates, Vietnam.
States Affected
NATIONWIDE
Quantity Affected
188 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0934-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.