Device adverse event reports (MAUDE)
Medical device reports of deaths, injuries and malfunctions sent to FDA by makers, facilities and the public. 26,849,547 records; openFDA updated it 2026-11-10. About this dataset
2 records match “semaglutide”
- Adverse Event Without Identified Device or Use Problem1
- Failure to Eject1
- Injury1
- Malfunction1
- WEGOVY (SEMAGLUTIDE) 2.4MG SINGLE DOSE PRE-FILLED PEN · INJECTOR, PEN
UNK · Failure to Eject
- OZEMPIC (SEMAGLUTIDE) INJECTION · NEEDLE, HYPODERMIC SINGLE LUMEN
NOVO-NORDISK A/S · Adverse Event Without Identified Device or Use Problem
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How to read this: Each report says someone told FDA an event happened while a product was used. A report does not show the product caused it, and counts rise and fall with how many people report. Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.