{"meta":{"dataset":"device-events","title":"Medical device adverse event reports by product code and quarter (FDA MAUDE via openFDA)","version":"1.0.0","doi":"10.5281/zenodo.23752988","doiUrl":"https://doi.org/10.5281/zenodo.23752988","conceptDoi":"10.5281/zenodo.23752987","license":"CC BY 4.0","licenseUrl":"https://creativecommons.org/licenses/by/4.0/","attribution":"Source: Probative, Medical device adverse event reports by product code and quarter (FDA MAUDE via openFDA), version 1.0.0, https://doi.org/10.5281/zenodo.23752988, licensed CC BY 4.0.","citation":"Probative. (2026). Medical device adverse event reports by product code and quarter (FDA MAUDE via openFDA) (Version 1.0.0) [Data set]. Zenodo. https://doi.org/10.5281/zenodo.23752988","disclaimer":"Not legal advice. A report to the FDA is an allegation that a device may have caused or contributed to an event, not a finding that it did, and a count of reports is not an incidence rate or proof of a defect. Questions about an injury from a medical device are for a licensed product-liability attorney and the person's doctor.","notice":"Probative is a marketing firm, not a law firm; not legal advice.","lastChecked":"2026-10-29","url":"https://probativegrowth.com/data/v1/device-events/changes.json","humanUrl":"https://probativegrowth.com/data/device-events/","statusCodes":{"P":"primary source","S":"secondary source","D":"ABA model default","U":"open question"}},"changes":[{"id":"device-events-2026-10-29-first","date":"2026-10-29","jurisdiction":"US","records":["device-events:US:2026Q3"],"status":"P","title":"Medical device adverse event reports by product code first published","summary":"FDA MAUDE adverse event reports by device product code and quarter, 2025Q1 to 2026Q3: 5,812,617 reports, with deaths, injuries and malfunctions for the 300 product codes with the most reports.","source":{"label":"openFDA device event API","url":"https://open.fda.gov/apis/device/event/"},"dataset":"device-events"}]}