The FDA has posted 7 enforcement recalls of non-heated anesthesia vaporizer devices since 2025, including 2 Class I (most serious) recalls. Most recent report: Dec 31, 2025.
A certain component of affected devices was not delivered within specification and contained impurities.
A certain component of affected devices was not delivered within specification and contained impurities.
Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.
Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.
Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.
Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.
Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.
Source: U.S. FDA openFDA device enforcement reports, updated continuously. Device type per the FDA's RES classification (“Vaporizer, Anesthesia, Non-Heated”). Informational only — verify against the FDA before acting.