# FDA recall Z-1074-2025

> **Getinge Usa Sales Inc** · Class I · device recall initiated 2025-01-15.

## Product

Vaporizer Sevoflurane, Quik-Fil. Model Number: 6682285.  Device is a component of Flow-i C20, Flow-i C30, Flow-i C40, Flow-c, Flow-e. For use during anesthesia.

## Reason for recall

Sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients or health care providers through inhalation and/or skin exposure. Potential harms include irritation of respiratory tract, which in worst case may lead to lung edema and/or severe hypocalcemia, blistering, superficial ulceration, and/or hypomagnesemia.

## Distribution

Domestic distribution to Kentucky and Connecticut.

## Key facts

- **Recall number:** Z-1074-2025
- **Recalling firm:** Getinge Usa Sales Inc
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-01-15
- **Report date:** 2025-02-19

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1074-2025

## Citation

> AI Analytics. FDA recall Z-1074-2025. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1074-2025. Source: US FDA. Licensed CC0.

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