3 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
FOOTSWITCH 1895420 XPS MULTIFUNCTION
FDA Adverse Event
Malfunction
·XOMED MFG JACKSONVILLE·Product code ERL·November 21, 2012
MINICAP
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·May 30, 2014
SETROX S 53
FDA Adverse Event
Malfunction
·BIOTRONIKE SE & CO. KG·Product code NVZ·September 17, 2010