8 results
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20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
CODMAN MIRROR FINISH BIPOLAR FORCEP
FDA Adverse Event
Malfunction
·JOHNSON & JOHNSON PROFESSIONAL, INC.·Product code GEI·November 17, 1999
CODMAN MIRROR FINISH BIPOLAR FORCEP
FDA Adverse Event
Malfunction
·JOHNSON & JOHNSON PROFESSIONAL, INC.·Product code GEI·November 17, 1999
ESSURE
FDA Adverse Event
BAYER HEALTHCARE LLC·Product code HHS·May 6, 2014
TI MIRS POLYAXIAL SCREW BODY
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code NKB·August 30, 2012
CAPSURE SP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 17, 2010
RICKHAM RESERVOIR
FDA Adverse Event
Injury
·JOHNSON AND JOHNSON PROFESSIONAL, INC. / MEDOS S.A·Product code JXG·November 20, 2015
SERVO-I
FDA Adverse Event
Malfunction
·MAQUET CRITICAL CARE AB·Product code CBK·April 12, 2023
VENT RES TR RICKHAM LG BA
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC.·Product code JXG·May 15, 2015