Medical device adverse event reports by product code and quarter (FDA MAUDE via openFDA)

Adverse event reports the FDA received about medical devices, counted by device product code and calendar quarter from 2025 Q1: reports, deaths, injuries, malfunctions and other, for the 300 product codes with the most reports and for all devices together. Counted with the openFDA device event API (licence CC0); no report row, narrative, patient or manufacturer is ever read, only counts. Reports are filed up to weeks after an event and are driven by litigation and recalls as well as by harm, so a count is not an incidence rate. 2079 records (status: P 2079). Canonical page: https://probativegrowth.com/data/device-events/. API: https://probativegrowth.com/data/v1/device-events/index.json. Published by Probative Growth (probativegrowth.com), a marketing agency for US law firms; not a law firm. 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.