Philips Panorama MRI Machine Recall Issued Over Explosion Risk
FDA has given the Philips Panorama MRI machine recall a Class I designation, indicating the devices put patients and others at risk of severe injury and death.
FDA has given the Philips Panorama MRI machine recall a Class I designation, indicating the devices put patients and others at risk of severe injury and death.
An estimated one out of every 250 patients who receive a gadolinium MRI contrast dye injection suffers hypersensitivity reactions, according to a recent study.
Injuries have been linked to the implantable devices failing to deliver therapy after they lost connection to patients' mobile devices after an MRI
A hack of the e-Alert MRI monitoring system could silence crucial alarms, putting patients at risk of serious injury or death, the CISA warns.
The FDA warns that lowered thyroid function in infants and children could lead to cognitive and developmental problems later in life.
Severe gadolinium-based contrast agent reactions could include heart rhythm problems and anaphylactic shock, researchers warn.