# FDA recall Z-0933-2026

> **Draeger, Inc.** · Class I · device recall initiated 2025-11-24.

## 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

- **Recall number:** Z-0933-2026
- **Recalling firm:** Draeger, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-11-24
- **Report date:** 2025-12-31

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Telford, PA, United States

## Primary source

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

## Citation

> AI Analytics. FDA recall Z-0933-2026. Retrieved 2026-07-28 from https://api.ai-analytics.org/recall/Z-0933-2026. Source: US FDA. Licensed CC0.

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