13 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
DXTEND SCREW LOCK D4.5X30MM
FDA Adverse Event
Malfunction
·DEPUY FRANCE S.A.S.-SAINT PRIEST ¿ REG. # 30038955·Product code KWS·June 25, 2014
UNIDENTIFIED ASR HEAD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KXA·July 6, 2015
UNKNOWN DEPUY ASR ACETABULAR CUP
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·January 2, 2013
KREULOCK SCREW, TI, 3.5X30
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HRS·August 4, 2025
LOCKING SCREW, TITANIUM 3.5MM X 22MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·April 18, 2019
LO-PRO SCRW,TI,3.5MMX 26MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·April 18, 2019
LO-PRO SCRW,TI,3.5MMX 38MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·April 18, 2019
LO-PRO SCRW,TI,3.5MMX 30MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·April 18, 2019
CALCANEAL FRAC PERIMETER PLT,XS,RT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·April 18, 2019
LO-PRO SCRW,TI,3.5MMX 24MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·April 18, 2019
LO-PRO SCRW,TI,3.5MMX 34MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·April 18, 2019
LO-PRO SCRW,TI,3.5MMX 36MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·April 18, 2019
LOCKING SCREW, TITANIUM 3.5MM X 28MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·April 18, 2019