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Maquet Critical Care AB recalls Servo-u MR Ventilator System. Model Number: 6888800.
Recalled July 9, 2025 · FDA recall Z-2015-2025 · Maquet Critical Care AB
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. · FDA Class I
Units
129 units
Sold at
US Nationwide distribution and Puerto Rico. No international distribution.
Description
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.
Product
Servo-u MR Ventilator System. Model Number: 6888800.
Manufacturer(s)
Maquet Critical Care AB
Made in
Sweden
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →