8 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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ALPHATEC
FDA Adverse Event
ALPHATEC MFG INC. AKA NEXMED INC·Product code HWC·February 26, 2004
STERNAL ZIPFIX WITH NEEDLE STERILE / 5 PACK
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code JDQ·April 23, 2013
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·April 29, 2011
RIATA ST OPTIM PASSIVE FIXATION LEAD
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·July 11, 2008
UNKNOWN HIP COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·January 29, 2025
VANGUARD SSK FEMORAL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·February 6, 2019
VANGUARD (TM) DCM TIBIAL BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·February 6, 2019
OSS TIBIAL POLY BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·January 13, 2025