United StatesDigitalDiagnost C90 Flex/Value/Chest/ER (Model 712035, UDI (01)00884838090705(21)24861049, Lot 24861049) distributed in the US to California; one unit is affected. The system was recalled because it was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.
What's being recalled
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Recalling firm: Philips North America Llc, Cambridge, MA, United States.
How to identify it
Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.
The hazard
System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.
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 distribution to California.
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)