31 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
3.5MM X 18.0MM LOCKING CORTICAL SCREW
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·March 5, 2012
3.5MM X 18.0MM LOCKING CORTICAL SCREW
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·March 5, 2012
.062" X 6" GUIDE WIRE
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·March 5, 2012
3.5MM X 26.0MM CORTICAL SCREW
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HRS·March 5, 2012
LPL LATERAL FIBULA PLATE 7H
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HRS·March 5, 2012
3.5MM X 40.0MM CORTICAL SCREW
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·March 5, 2012
3.5MM X 22.0MM CORTICAL SCREW
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·March 5, 2012
.062" X 6" GUIDE WIRE
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·March 5, 2012
3.5MM X 16.0MM LOCKING CORTICAL SCREW
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·March 5, 2012
3.5MM X 20.0MM CORTICAL SCREW
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·March 5, 2012
.062" X 6" GUIDE WIRE
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·March 5, 2012
3.5MM X 38.0MM CORTICAL SCREW
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·March 5, 2012
3.5MM X 12.0MM LOCKING CORTICAL SCREW
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·March 5, 2012
3.5MM X 20.0MM LOCKING CORTICAL SCREW
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·March 5, 2012
3.5MM X 38.0MM LOCKING CORTICAL SCREW
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·March 5, 2012
3.5MM X 40.0MM CORTICAL SCREW
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·March 5, 2012
3.5MM X 12.0MM LOCKING CORTICAL SCREW
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·March 5, 2012
4.0MM X 40.0MM CANCELLOUS SCREW
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·March 5, 2012
4.0MM X 14.0MM CANCELLOUS SCREW
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·March 5, 2012
STERIS C-MAX 110
FDA Adverse Event
Other
·STERIS CORP·Product code FQO·March 8, 2013