20 results
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40ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
3.0MM TI CANNULATED SCREW LONG THREAD/32MM
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code HWC·June 12, 2014
3.0MM TI CANNULATED SCREW SHORT THREAD/32MM
FDA Adverse Event
Malfunction
·SYNTHE USA·Product code HWC·June 12, 2014
1.1MM THREADED GUIDE WIRE 150MM
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code FZX·June 12, 2014
1.1MM THREADED GUIDE WIRE 150MM
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code FZX·June 12, 2014
1.1MM THREADED GUIDE WIRE 150MM
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code FZX·June 12, 2014
1.1MM THREADED GUIDE WIRE 150MM
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code FZX·June 12, 2014
3.0MM TI CANNULATED SCREW SHORT THREAD/20MM
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code HWC·June 12, 2014
1.1MM THREADED GUIDE WIRE 150MM
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code FZX·June 12, 2014
2.0MM CANNULATED DRILL BIT/QC 150MM
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code HWE·June 12, 2014
CRUCIFORM SCREWDRIVER SHAFT
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code HXX·June 12, 2014
1.1MM NON-THREADED GUIDE WIRE 150MM
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code FZX·June 12, 2014
3.0MM TI CANNULATED SCREW
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code HWC·June 12, 2014
1.1MM THREADED GUIDE WIRE 150MM
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code FZX·June 12, 2014
3.0MM TI CANNULATED SCREW SHORT THREAD/34MM
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code HWC·June 12, 2014
1.1MM NON-THREADED GUIDE WIRE 150MM
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code FZX·June 12, 2014
3.0MM TI CANNULATED SCREW SHORT THREAD/15MM
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code HWC·June 12, 2014
3.0MM TI CANNULATED SCREW SHORT THREAD/15MM
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code HWC·June 12, 2014
LYNX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·February 14, 2013
DEPUY ASR XL FEM IMP SIZE 47
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·January 7, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2014