6 results
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37ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ORTHO SUMMIT TM SAMPLE HANDLING SYSTEM
FDA Adverse Event
Malfunction
·HAMILTON BONADUZ AG·Product code JTC·August 18, 2000
ALLOFT-S ALLOCLASSIC SHL 52/II
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code JDI·March 12, 2019
SURGICEL ABSORBABLE HEMOSTAT
FDA Adverse Event
Injury
·ETHICON, INC.·Product code LMG·March 14, 2013
RESTORE PRIME
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·February 24, 2011
3004659744-2008-00003
FDA Adverse Event
Injury
·Product code JAK·February 8, 2008
ALLOFIT-S ALLOCLASSIC, SHELL WITH POLAR SCREW PLUG, UNCEMENTED, 52/II
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LZO·September 27, 2018