The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
• Devices Recalled in the U.S.: 150
The Panorama 1.0T is a magnetic resonance (MR) system, a machine used to take different kinds of images. These images show what's inside the body and can help health care providers make a…
This story from fda.gov was posted on 2023-12-21 by @hazelpine.