Class I

Medical Device Recall: Servo-u MR Ventilator System. Model Number: 6888800.

Maquet Critical Care AB · May 30, 2025

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.

States Affected

NATIONWIDE

Quantity Affected

129 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2015-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Maquet Critical Care AB Medical Device Recall: Servo-u MR Ventilator System. Model Number: 6888800. | SafeCheck