Medivance, Inc. ¿ 1725056
FDA adverse event reports naming Medivance, Inc. ¿ 1725056 as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDIVANCE, INC. ¿ 1725056.
Total reports
21,244
Breakdown unavailable for this manufacturer. FDA filed these reports under a name containing characters the openFDA search API cannot match, so the death, injury and malfunction split, the yearly trend and the device categories can't be retrieved. The total above comes from openFDA's manufacturer index, which does return the name.
This is a limitation of the FDA's public API, not a gap in the underlying reports.
Monitor Medivance, Inc. ¿ 1725056 automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.