FDA · Medical devices ·
GETINGE Y SENSOR Module recall
Maquet Critical Care AB recalled GETINGE Y SENSOR Module on August 26, 2026 because of the module did not undergo electrical safety tests and functional tests during production. It was sold nationwide.
Why it was recalled
The module did not undergo electrical safety tests and functional tests during production.
What's recalled
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.
Quantity: 9 units
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Maquet Critical Care AB, Solna
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
US Nationwide distribution in the states of CA, GA, MN, NY. - Status
- Ongoing
- Recall number
- Z-2963-2026
- Source
- U.S. Food and Drug Administration
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