United StatesThe recalled product is the GETINGE Y SENSOR Module (Model 6693662) used as part of the SERVO‑U/-N continuous ventilator system for facility use, identified by DUI/DI 07325710000304 and serial/lot numbers 21049, 21088, 21089, 21093, 21100, 21103, 21108, 21114, and 21115. Maquet Critical Care AB recalled nine units because the modules did not undergo electrical safety tests and functional tests during production; affected units were distributed in CA, GA, MN, and NY.
What's being 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.
Recalling firm: Maquet Critical Care AB, Solna, Sweden.
How to identify it
DUI/DI 07325710000304, Serial/Lot Numbers: 21049, 21088, 21089, 21093, 21100, 21103 21108, 21114, 21115.
The hazard
The module did not undergo electrical safety tests and functional tests during production.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide distribution in the states of CA, GA, MN, NY.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)