10 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·February 21, 2025
PERCLOSE PROGLIDE¿
FDA Adverse Event
Injury
·ABBOTT VASCULAR INC.·Product code MGB·December 9, 2024
4 FR S/L GROSHONG NXT CLEARVUE BASIC KIT W/MICROINTRODUCER
FDA Adverse Event
Malfunction
·C. R. BARD INC. (BASD)·Product code LJS·March 7, 2013
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 25, 2011
SELUTE PICOTIP LEAD
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS, INC·Product code DTB·May 8, 2008
COCR FEMORAL HEAD
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·November 6, 2019
XLPE LINER ELEVATED RIM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·November 6, 2019
TRILOGY SHELL
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·November 6, 2019
STARCLOSE SE
FDA Adverse Event
Injury
·ABBOTT VASCULAR INC.·Product code MGB·September 18, 2024
PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code NIQ·February 4, 2011