16 results
·
31ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
BILOX PROSTHESIS HEAD 12/14 28MM L
FDA Adverse Event
Malfunction
·AESCULAP AG AND CO. KG·Product code LWJ·May 23, 2014
EXCIA L PLASMAPORE UCAP 8/10 SIZE 11MM
FDA Adverse Event
Malfunction
·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014
ISODUR PROSTHESIS HEAD 12/14 32MM L
FDA Adverse Event
Malfunction
·AESCULAP AG&CO KG·Product code LPH·August 7, 2014
QUINTEX SEMICONSTRAINED SCREW 4.0X16MM
FDA Adverse Event
Malfunction
·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014
BIOLOX PROSTHESIS HEAD 12/14 28MM S
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code LWJ·April 27, 2012
EXCIA PLASMAPORE-UCAP 8/10 SIZE 11MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code MEH·June 21, 2013
EXCIA CEMENTED 8/10 SIZE 12MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code JDI·November 5, 2012
BIOLOX PROSTHESIS HEAD 12/14 28MM S
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code LWJ·April 14, 2014
BIOLOX PROSTHESIS HEAD 12/14 28MM M
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code LWJ·April 27, 2012
BIOLOX PROSTHESIS HEAD 12/14 32MM L
FDA Adverse Event
Malfunction
·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014
BIOLOX PROSTHESIS HEAD 8/10 32MM M
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code LZO·June 21, 2013
BIOLOX PROSTHESIS HEAD 12/14 28MM S
FDA Adverse Event
Malfunction
·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 29, 2013
NEXGEN FEMORAL PROVISIONAL IMPACTOR EXTRACT
FDA Adverse Event
Malfunction
·ZIMMER, INC.·Product code MBH·April 5, 2011
OUTBACK RE-ENTRY CATHETER
FDA Adverse Event
Malfunction
·CORDIS DE MEXICO·Product code DQY·July 22, 2008
ISODUR PROSTHESIS HEAD 12/14 28MM M
FDA Adverse Event
Malfunction
·AESCULAP AG AND CO. KG·Product code LPH·January 16, 2015