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Recall Observatory FDA recall evidence

Device product

Sevoflurane E_Vap.(Quik-Fil):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 115-066755-00

Z-2949-2024

July 22, 2024

Class II

Product summary

Firm
Mindray DS USA, Inc. dba Mindray North America
Event
Event 95099
Status
Ongoing
Classification
Class II
Quantity
2 units
Official record key
device-enforcement:Z-2949-2024

Official wording

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

Code information: UDI-DI: 06936415975784 Serial Number: AH6D28000517, AH6D28000518

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

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    incomplete seal