Reporting Problems with Medical Devices

Under current FDA regulations, manufacturers and distributors of medical devices, and medical facilities that use them, must report any event that may have resulted in an injury, serious illness, or death within five days of the event. The FDA also maintains a volunteer reporting system called MedWatch where medical professionals and consumers can report adverse events with devices, over-the-counter drugs and devices, and prescription drugs. If you have been injured while using or being treated with a medical device, time is of the essence. Consulting with a personal injury lawyer about any time limits or reporting requirements can be crucial if you have been injured.