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Maquet Critical Care AB Recalls
4 recalls on record · July 9, 2025 to August 12, 2026 · Medical Devices
Recalls by year
25
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
August 12, 2026Medical DevicesFDA
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 68
Hazard: 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 intraoperative awareness.
July 9, 2025Medical DevicesFDA
Maquet Critical Care AB recalls Servo-u MR Ventilator System. Model Number: 6888800.
Hazard: 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.
July 9, 2025Medical DevicesFDA
Maquet Critical Care AB recalls Servo-n Ventilator System. Model Number: 6694800.
Hazard: 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.
July 9, 2025Medical DevicesFDA
Maquet Critical Care AB recalls Servo-u Ventilator System. Model Number: 6688600.
Hazard: 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.