11 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PERSONA ARTICULAR SURFACE
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code MBH·May 5, 2016
HUDSON OPTI-NEB PRO COMPRESSOR W/DISP NEB.
FDA Adverse Event
Malfunction
·TELEFLEX·Product code CAF·March 8, 2013
TOTALCARE
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·February 3, 2011
FREESTYLE
FDA Adverse Event
Injury
·ABBOTT DIABETES CARE INC, USA·Product code LFR·February 15, 2008
PERSONA CEMENTED STEMMED TIBIAL PLATE
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code JWH·October 31, 2016
PERSONA CEMENTED POSTERIOR FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code JWH·October 31, 2016
UNFOLDER PLATINUM 1 SERIES
FDA Adverse Event
Malfunction
·AMO PUERTO RICO MFG. INC.·Product code KYB·January 8, 2025
UNFOLDER PLATINUM 1 SERIES
FDA Adverse Event
Malfunction
·AMO PUERTO RICO MFG. INC.·Product code KYB·January 8, 2025
UNFOLDER PLATINUM 1 SERIES
FDA Adverse Event
Malfunction
·AMO PUERTO RICO MFG. INC.·Product code KYB·January 8, 2025
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·November 13, 2015
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·September 22, 2016