Class IIOngoingZ-2963-2026
Maquet Critical Care AB recalls GETINGE Y SENSOR Module
The module did not undergo electrical safety tests and functional tests during production.
Maquet Critical Care A…Aug 26, 2026
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–2 of 2 recalls
The module did not undergo electrical safety tests and functional tests during production.
Events observed where anesthetic agent was not delivered when the vaporizer was activated. Failure to deliver the anesthetic agent may result in the patient receiving insufficient anesthesia and may lead to intraoperativ…