3 results
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17ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
DEPUY ASR XL FEM IMP SIZE 49
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·January 30, 2013
ENDOPATH** XCEL*
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·December 22, 2010
M2A-RLOC LNR 10 DEG SZ 24/28MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·July 15, 2014