Coils Recalled Due to a Potential Issue
Philips North America LLC is updating use instructions for SENSE XL Torso (1.5T and 3.0T) coils due to a Potential Issue Where the Coil Heats Up During MRI Scans, Possibly Leading to Thermal Injury.
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices without following the updated instructions may cause serious injuries or death.
