4 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
LEXINGTON MEM W COLUMBIA SC 2
FDA Adverse Event
Other
·SORIN GROUP USA, INC.·Product code DTZ·October 30, 2013
COBLATOR II
FDA Adverse Event
Injury
·ARTHROCARE CORPORATION·Product code GEI·June 13, 2014
ZELTIQ COOLMAX (8.0)
FDA Adverse Event
Injury
·ZELTIQ AESTHETICS INC.·Product code OOK·January 8, 2013
INTEGRATED APD SET W/CASSETTE3-PRONG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·December 2, 2010