Class II
Medical Device Recall: GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662; part of the SERVO-U/-N continuous ventilator system, for facility use. Maquet Critical Care AB, is a subsidiary of Getinge.
Maquet Critical Care AB · June 30, 2026
Reason for Recall
The module did not undergo electrical safety tests and functional tests during production.
Distribution
US Nationwide distribution in the states of CA, GA, MN, NY.
States Affected
NATIONWIDE
Quantity Affected
9 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2963-2026
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.