Maquet Critical Care AB recalls GETINGE Y SENSOR Module
- Recalling company
- Maquet Critical Care AB
- Product
- 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.
- Reason
- The module did not undergo electrical safety tests and functional tests during production.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jun 30, 2026
- Reported
- Aug 26, 2026
- Distribution
- US Nationwide distribution in the states of CA, GA, MN, NY.
- Status
- Ongoing
- Quantity
- 9 units
- Lot / codes
- DUI/DI 07325710000304, Serial/Lot Numbers: 21049, 21088, 21089, 21093, 21100, 21103 21108, 21114, 21115.
- Company location
- Solna
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2963-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2963-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.