8 results
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36ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
GMK-REVISION FIXED TIBIAL INSERT SC SIZE 3/17MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·March 14, 2024
CONSERVE(R) PLUS CUP
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LZO·August 12, 2024
GMK REVISION TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·January 2, 2025
PENUMBRA SMART COIL DETACHMENT HANDLE
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code HCG·August 7, 2017
PENUMBRA SMART COIL
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code HCG·August 7, 2017
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·March 13, 2013
PLASMABLADE TNA TISSUE DISSECTION DEVICE
FDA Adverse Event
Other
·PEAK SURGICAL INC.·Product code GEI·February 18, 2011
GE OEC 9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC·Product code JAA·February 22, 2008