4 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
VACUETTE BLOOD COLLECTION TUBE 3ML K2E K2EDTA
FDA Adverse Event
Malfunction
·GREINER BIO-ONE NA INC.·Product code JKA·November 2, 2020
SPRINT FIDELIS
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·January 26, 2011
M2A-MAGNUM MOD HD SZ 52MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·July 31, 2014
BIOSENSE WEBSTER NAVISTAR DS RMT DIAGNOSTIC/ABLATION STEERABLE CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC.·Product code LPB·September 7, 2007