3 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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ASR UNI FEMORAL IMPL SIZE 47
FDA Adverse Event
Injury
·DEPUY INTL., LTD - 8010379·Product code KWA·June 5, 2014
SPINBRUSH PRO WHITENING POWERED TOOTHBRUSH
FDA Adverse Event
Malfunction
·CHURCH & DWIGHT CO., INC.·Product code JEQ·November 13, 2012
LAMITRODE 44 LEAD
FDA Adverse Event
Injury
·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·September 29, 2010