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FDA (Device enforcement)Recalled 2025-05-30class i

Maquet Critical Care AB: 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.

Details from the source

Reason for recall: 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. Distribution: US Nationwide distribution and Puerto Rico. No international distribution. Quantity: 129 units Lot/code info: Model Number: 6888800. UDI-DI: 07325710010518. All software versions.

UPC codes

07325710010518

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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