16 results · 31ms · Sources: EU EUDAMED, US FDA

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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