11 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code LIT·December 1, 2006
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP.·Product code DQY·March 27, 2007
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code DQY·December 28, 2006
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP.·Product code DQY·March 5, 2007
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 28, 2006
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORP.·Product code DQY·April 12, 2007
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HXX·April 3, 2013
HOYER LIFT
FDA Adverse Event
Other
·APEX HEALTHCARE MFG INC.·Product code FNG·March 21, 2011
CONTOUR TS TEST STRIPS (50)
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE LLC·Product code NBW·April 15, 2008
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·April 15, 2022
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·September 21, 2017