Women who received repeated Depo-Provera shots may need regular MRI and CT scans to watch for the development of brain tumors, medical monitoring lawsuit claims.
Depo-Provera lawsuit claims woman may eventually lose control of her tongue due to a tumor that cannot be surgically removed.
Even after extensive brain surgery, the Depo-Provera brain tumor could return, resulting in a need for yearly MRIs and potential radiation therapy.
Indiana woman must undergo MRI tests every one to two years to monitor the growth of a brain tumor caused by the Depo-Provera shot, according to complaint.
Despite multiple burn injuries to users, the manufacturer is not pulling the recalled SENSE XL Torso devices from the market.
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.
