---
title: "Sevoflurane E_Vap.(Safety Filling adapter) used with the A9 Anesthesia System... — FDA record Z-2950-2024 | Is It on Recall"
description: "V90 electronic vaporizer anesthetic agent output may be higher than the set amount due to a component within the vaporizer causing an incomplete seal in some ca"
url: https://isitonrecall.com/recall/fda-device-z-2950-2024-sevoflurane-e-vap-safety-filling-adapter-used-with-the-a9-anesthesia-system-used-to-provide-the-vapo/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Sevoflurane E\_Vap.(Safety Filling adapter) used with the A9 Anesthesia System-Used to provide the vapor of an anesthe... — FDA record Z-2950-2024

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 Jul 22, 2024. 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**: Sevoflurane E\_Vap.(Safety Filling adapter) used with the A9 Anesthesia System-Used to provide the vapor of an anesthetic agent with controllable concentration to an A9 anesthesia system. Part Number: 115-066756-00
- **Reason**: V90 electronic vaporizer anesthetic agent output may be higher than the set amount due to a component within the vaporizer causing an incomplete seal in some cases. Should this issue occur, the A9 Anesthesia System will generate alarms associated with abnormal vaporizer output. If the anesthetic concentration is too high, the patient can inhale too much anesthetic agent; the patient may suffer from symptoms such as vertigo and drowsiness after the operation. In severe cases, the patient may suffer from neurological sequelae such as hypomnesia and inattention
- **Classification**: Class II
- **Recalling firm**: Mindray DS USA, Inc. dba Mindray North America
- **Quantity**: 96 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2950-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2950-2024%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 | UDI-DI: 06936415975777 Serial Number: AH6A28000471 AH6A24000202 AH6A28000474 AH6A27000378 AH6A28000466 AH6A24000195 AH6A28000457 AH6A25000237 AH6A28000426 AH6A24000199 AH6A24000207 |

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

## Distribution

US Distribution to states of: California, Georgia, Kentucky, Mississippi, New Jersey, Puerto Rico, Texas, and West Virginia; and International (Foreign) to: Canada

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

- [California](https://isitonrecall.com/state/california/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Kentucky](https://isitonrecall.com/state/kentucky/)
- [Mississippi](https://isitonrecall.com/state/mississippi/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [Texas](https://isitonrecall.com/state/texas/)
- [West Virginia](https://isitonrecall.com/state/west-virginia/)

## Dates in the source

- **Report date**: Sep 11, 2024
- **Recall initiation date**: Jul 22, 2024
- **Center classification date**: Sep 4, 2024

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-2950-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Mindray DS USA, Inc. dba Mindray North America records](https://isitonrecall.com/brand/mindray-ds-usa-inc-dba-mindray-north-america/)