6 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TIBIAL NAIL, STANDARD T2 TIBIA 9X300 MM
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·October 12, 2012
DXTEND GLENOSPHERE ECC D42MM
FDA Adverse Event
Injury
·DEPUY FRANCE S.A.·Product code KWS·November 14, 2008
TOSHIBA
FDA Adverse Event
Injury
·TOSHIBA AMERICA MEDICAL SYSTEMS·Product code LNH·September 2, 2011
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 18, 2013
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·October 3, 2016
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HRS·August 26, 2016