4 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
URIC ACID REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code KNK·April 15, 2011
UNKNOWN ASR CUP
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·December 21, 2012
QUATTRODE 3/6 PERCUTANEOUS LEADS
FDA Adverse Event
Malfunction
·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·October 19, 2010
OMNIPOD INSULIN PUMP
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code LZG·February 20, 2014