Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer.
Reported: December 31, 2025 Initiated: November 24, 2025 #Z-0933-2026
Product Description
Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer.
Reason for Recall
A certain component of affected devices was not delivered within specification and contained impurities.
Details
- Recalling Firm
- Draeger, Inc.
- Units Affected
- 431 units
- 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.
- Location
- Telford, PA
Frequently Asked Questions
What product was recalled? ▼
Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer.. Recalled by Draeger, Inc.. Units affected: 431 units.
Why was this product recalled? ▼
A certain component of affected devices was not delivered within specification and contained impurities.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 31, 2025. Severity: Critical. Recall number: Z-0933-2026.
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