---
title: "Vaporizer Sevoflurane, Quik-Fil. Model Number: 6682285. Device is a component... — FDA record Z-1074-2025 | Is It on Recall"
description: "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"
url: https://isitonrecall.com/recall/fda-device-z-1074-2025-vaporizer-sevoflurane-quik-fil-model-number-6682285-device-is-a-component-of-flow-i-c20-flow-i-c30-f/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Vaporizer Sevoflurane, Quik-Fil. Model Number: 6682285. Device is a component of Flow-i C20, Flow-i C30, Flow-i C40, ... — FDA record Z-1074-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jan 15, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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**: 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.
- **Classification**: Class I
- **Recalling firm**: Getinge Usa Sales Inc
- **Quantity**: 6 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1074-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1074-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Model Number: 6682285. UDI-DI: 07325710001141. Serial Numbers: 3761, 7635, 7633, 7630, 7632, 7631. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Domestic distribution to Kentucky and Connecticut.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Connecticut](https://isitonrecall.com/state/connecticut/)
- [Kentucky](https://isitonrecall.com/state/kentucky/)

## Dates in the source

- **Report date**: Feb 19, 2025
- **Recall initiation date**: Jan 15, 2025
- **Center classification date**: Feb 7, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1074-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Getinge Usa Sales Inc records](https://isitonrecall.com/brand/getinge-usa-sales-inc/)