9 results
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44ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
S-ICD SYSTEM
FDA Adverse Event
Malfunction
·CAMERON HEALTH·Product code LWS·November 28, 2015
S-ICD SYSTEM
FDA Adverse Event
Injury
·CAMERON HEALTH INC.·Product code LWS·October 23, 2014
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·January 11, 2013
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-REDWOOD CITY·Product code MGB·December 1, 2010
11MM/130 DEG TI CANN TROCH FIXATION NAIL 360MM/LEFT-STER
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code JDS·July 3, 2014
ATLANTIS SR PRO2 CORONARY IMAGING CATHETER, MODEL 39014
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - FREMONT·Product code DQO·May 18, 2011
ATLANTIS SR PRO2 CORONARY IMAGING CATHETER, MODEL 39014
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - FREMONT·Product code DQO·April 18, 2011
ATLANTIS SR PRO2 CORONARY IMAGING CATHETER, MODEL 39014
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - FREMONT·Product code DQO·May 5, 2011
ATLANTIS SR PRO2 CORONARY IMAGING CATHETER, MODEL 39014
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - FREMONT·Product code DQO·April 26, 2011