17 results
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33ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
MAESTRO 4000 CONTROLLER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code LPB·April 25, 2023
MAESTRO FOOT SWITCH
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 6, 2018
MAESTRO 4000 CONTROLLER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code LPB·September 29, 2025
MAESTRO 4000 CONTROLLER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code LPB·November 3, 2023
MAESTRO 4000 CONTROLLER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 7, 2023
AFX
FDA Adverse Event
Malfunction
·ENDOLOGIX, INC.·Product code MIH·January 22, 2016
MAESTRO 4000 POD, 100W
FDA Adverse Event
Malfunction
·STELLARTECH RESEARCH CORPORATION·Product code LPB·August 17, 2023
MAESTRO 4000 CONTROLLER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code LPB·October 2, 2023
NEXGEN LPS-FLEX GSF FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·April 3, 2013
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·March 9, 2011
ANT-CER 2 LVL PLATE ASSY, 44MM
FDA Adverse Event
Injury
·Product code KWQ·May 7, 2008
3I T3® NON-PLATFORM SWITCHED TAPERED IMPLANT 5 X 10MM
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code DZE·March 12, 2018
3I T3® NON-PLATFORM SWITCHED TAPERED IMPLANT 5 X 10MM
FDA Adverse Event
Injury
·BIOMET 3I·Product code DZE·January 27, 2020
IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LGW·October 8, 2019
NEU_INTERSTIM_INS
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code EZW·July 12, 2012
3I T3® NON-PLATFORM SWITCHED TAPERED IMPLANT 5 X 13MM
FDA Adverse Event
Injury
·BIOMET 3I·Product code DZE·March 31, 2020
3I T3® NON-PLATFORM SWITCHED TAPERED IMPLANT 5 X 10MM
FDA Adverse Event
Injury
·BIOMET 3I·Product code DZE·July 31, 2019