Class I

Medical Device Recall: Servo-u Ventilator System. Model Number: 6688600.

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

874 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2013-2025

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.