FDA recall Z-0933-2026

Draeger, Inc. · Class I · device

Product

Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer.

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.

Key facts

Status
Ongoing
Initiation date
2025-11-24
Report date
2025-12-31
Voluntary/Mandated
Voluntary: Firm initiated
Location
Telford, PA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0933-2026