United StatesThe Philips Incisive CT imaging system manufactured by Philips Healthcare (Suzhou) Co., Ltd., sold in the U.S. and U.S. territories (35 units), is affected. It was recalled because an unstable connection inside the floating sensor can cause incomplete scans.
What's being recalled
Philips Incisive CT
Recalling firm: Philips Healthcare (Suzhou) Co., Ltd., Suzhou, China.
The hazard
Potential for incomplete scan due to unstable connection inside of floating sensor.
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
U.S. and U.S. territories
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)