Official recall notice
FDA DeviceClass IINotable
FDA Recall: GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662; part of the SERVO-U/-N continuous v
- Recall date
- 2026-08-26
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
The module did not undergo electrical safety tests and functional tests during production.
Product description
The module did not undergo electrical safety tests and functional tests during production.
Affected products
DUI/DI 07325710000304, Serial/Lot Numbers: 21049, 21088, 21089, 21093, 21100, 21103 21108, 21114, 21115.