Draeger, Inc. recalls Draeger Vapor 3000. Unheated, calibrated anesthetic vaporizer.

Recall date

November 24, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0934-2026

FDA classification

Class I

Brand / firm

Draeger, Inc.

Sold / distributed

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, Is…

Why it was recalled

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

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

Draeger Vapor 3000. Unheated, calibrated anesthetic vaporizer.