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Draeger, Inc. recalls Draeger Vapor 3000. Unheated, calibrated anesthetic vaporizer.
Recalled December 31, 2025 · FDA recall Z-0934-2026 · Draeger
Hazard
A certain component of affected devices was not delivered within specification and contained impurities. · FDA Class I
Units
188 units
Sold at
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.
Description
A certain component of affected devices was not delivered within specification and contained impurities.
Product
Draeger Vapor 3000. Unheated, calibrated anesthetic vaporizer.
Manufacturer(s)
Draeger, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →