United StatesPhilips North America is recalling Cardiac Workstation 5000 (Model 860439, UDI-DI 00884838094826) and Cardiac Workstation 7000 (Model 860441, UDI-DI 00884838094833; serials include US42520284, US32520248, US32520244, US22520238, US22520221) distributed in CA, IA, TN, TX and VA (28 and 29 units respectively). The devices were recalled after failure of Environmental Stress Testing found a pinched power module wire inside the housing that resulted in a short.
What's being recalled
Cardiac Workstation 5000; Model Number: 860439;
Cardiac Workstation 7000; Model Number: 860441;
Recalling firm: Philips North America, Cambridge, MA, United States.
How to identify it
Model Number: 860439; UDI-DI: 00884838094826; Serial Numbers: Model Number: 860441; UDI-DI: 00884838094833; Serial Numbers: US42520284, US32520248, US32520244, US22520238, US22520221;
The hazard
Failure of Environmental Stress Testing from a pinched power module wire within the housing of the Cardiac Workstation device which resulted in a short.
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, IA, TN, TX, VA.
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)