# FDA recall Z-1497-2025

> **Draeger, Inc.** · Class I · device recall initiated 2025-03-12.

## Product

Brand Name: Anesthesia Circuit Kit  Product Name: Anesthesia Circuit Kit Flex 6  Model/Catalog Number: MP02744  Software Version: Not applicable  Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended for single use only

## Reason for recall

The potential for cracks forming in the breathing circuit hose.

## Distribution

Domestic: Nationwide Distribution.  International - following countries: Austria, Belgium, Bulgaria, China, Croatia, Czech Republic, France, Germany, Ghana, Greece, Guatemala, Hungary, India, Italy, Japan, Panama, Philippines, Portugal, Singapore, South Africa, Spain, Sweden, United Kingdom

## Key facts

- **Recall number:** Z-1497-2025
- **Recalling firm:** Draeger, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-03-12
- **Report date:** 2025-04-09

- **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-1497-2025

## Citation

> AI Analytics. FDA recall Z-1497-2025. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/Z-1497-2025. Source: US FDA. Licensed CC0.

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