Reported Reactions

Adverse event reports that FDA received

  • Search
  • Watch list

Devices by type

FDA gives each type of device a product code. A device type has a page when 300 or more reports have its code. Search engines may index the pages of the types with 5,000 reports or more. The page of a type lists each brand name of the type. The data have the reports that FDA received through .

FDA says:

MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices.

Source: openFDA, Manufacturer and User Facility Device Experience. The site read the page on .

1,071 device types, in 4 parts

1,982 brand names, in 7 parts

These are the brand names with 1,000 or more reports. Each other brand name has a page too, and the page of its device type lists it. Search engines may index the pages with 3,000 reports or more, and 50 or more in the latest 12 months.

Manufacturers named on the reports

Brand names with no device type page

These 43 brand names have a page, and their product code has no page.