Medical Device Report (MDR)

/ˈɛmɛdiəkeɪəɛl diɪˈvaɪɛs ɑrɪˈpiɔrt (ɛɛm-di-ɑɑr)/

A report submitted to the FDA by a manufacturer, a physician, or a patient about a marketed device that may have caused or contributed to a death or serious injury. A report can be submitted at the following link: https://www.fda.gov/medicaldevices/safety/reportaproblem/default.htm