Draeger, Inc.: Device Recall

Recall #Z-0934-2026 · 11/24/2025

Class I: Dangerous

Recall Details

Recall Number
Z-0934-2026
Classification
Class I
Product Type
Device
Recalling Firm
Draeger, Inc.
Status
Ongoing
Date Initiated
11/24/2025
Location
Telford, PA, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
188 units

Reason for Recall

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

Product Description

Draeger Vapor 3000. Unheated, calibrated anesthetic vaporizer.

Distribution Pattern

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.

Other Recalls by Draeger, Inc.

View all recalls by Draeger, Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.