Sevoflurane, Desflurane, And Isoflurane Electronic Vaporizer Material Package

Recall Summary Electronic vaporizer material packages used to deliver sevoflurane, desflurane, and isoflurane (anesthetic gases) are being recalled across Canada due to performance issues. These products are used in hospitals and surgical facilities during anesthesia administration. The FDA classified this as a Class I recall, indicating a serious potential health hazard.

Product
Sevoflurane, Desflurane, and Isoflurane Electronic Vaporizer Material Package
Reason
Performance
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2024-11-15
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/fa9ca346-657c-4148-a938-9664dd4847df