8 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
NEXGEN COMPLETE KNEE SOLUTION LEGACY KNEE-CONSTRAINED CONDYL
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·September 24, 2004
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECES
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 8, 2006
NEXGEN LCCK FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·December 21, 2012
ECLIPSE FILTER SYSTEM
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·March 5, 2013
VERTE-STACK SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·Product code MQP·February 16, 2011
CAPSURE Z
FDA Adverse Event
Injury
·MPRI·Product code DTB·August 8, 2014
STAINLESS STEEL K-WIRE 1.6MM
FDA Adverse Event
Malfunction
·BIOMET TRAUMA·Product code HTY·June 22, 2017
OPTIPAC 80 REFOBACIN REVISION
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code MBB·January 24, 2022