# FDA recall Z-0720-2026

> **Mindray DS USA, Inc. dba Mindray North America** · Class II · device recall initiated 2025-10-20.

## Product

Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the following:    1. Sev E_Vap. (Safety Filling adapter), Part Number: 115-066756-00.     2. Exchange Sev E_Vap. (Safety Filling adapter), Part Number: E115-066756-00.    Product Description: The Anesthesia System is a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic and to maintain a patient's ventilation. The A9 Anesthesia System utilizes V90 electronic vaporizers for anesthetic agent delivery.

## Reason for recall

Potential for anesthesia leakage.

## Distribution

Worldwide - US Nationwide distribution in the states of California, Florida, Georgia, Kentucky, Maryland, Mississippi, Missouri, New Jersey, Puerto Rico, Texas, Washington, West Virginia and the country of Canada.

## Key facts

- **Recall number:** Z-0720-2026
- **Recalling firm:** Mindray DS USA, Inc. dba Mindray North America
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-10-20
- **Report date:** 2025-12-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mahwah, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0720-2026

## Citation

> AI Analytics. FDA recall Z-0720-2026. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0720-2026. Source: US FDA. Licensed CC0.

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