Maquet Critical Care AB recalls
3 official recalls and safety alerts involving Maquet Critical Care AB since 2025-07, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Maquet Critical Care AB or the relevant agency.
- 2026-08-26
USMaquet Critical Care AB recalls GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662; part of the SERVO-U/-N continuous ventilator system, for facility use.…
The module did not undergo electrical safety tests and functional tests during production.
FDA · DeviceMaquet Critical Care ABUS Nationwide distribution in the states of CA, GA, MN, NY.Official notice →- 2026-08-12
- US
Maquet Critical Care AB recalls Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30 6888530 Flow-i C40 6888540…
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…
FDA · DeviceMaquet Critical Care ABWorldwide - US Nationwide distribution to the states of AL, AR, CA, CO, DC,…Official notice → - 2025-07-09
- US
Maquet Critical Care AB recalls Servo-u Ventilator System. Model Number: 6688600.
Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.
FDA · DeviceMaquet Critical Care ABUS Nationwide distribution and Puerto Rico. No international distribution.Official notice →