1,273 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·March 4, 2010
COBAS 6000 E601 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CEM·June 8, 2010
ANALYTICAL P MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·March 22, 2010
ANALYTICAL P MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·February 16, 2010
KYPHX® HV-R¿ BONE CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SPINE LLC·Product code NDN·December 6, 2010
ELEOS LIMB SALVAGE SYSTEM
FDA Adverse Event
Injury
·ONKOS SURGICAL·Product code KRO·October 24, 2024
ELEOS LIMB SALVAGE SYSTEM
FDA Adverse Event
Injury
·ONKOS SURGICAL·Product code KRO·October 24, 2024
STERILE LUBRICATING JELLY
FDA Adverse Event
Injury
·H AND P INDUSTRIES, INC.·Product code KMJ·August 12, 2023
STERILE LUBRICATING JELLY
FDA Adverse Event
Injury
·H AND P INDUSTRIES, INC.·Product code KMJ·August 12, 2023
ELEOS
FDA Adverse Event
Death
·ONKOS SURGICAL·Product code KRO·January 18, 2024
COBAS 6000 C501MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JGS·March 30, 2010
UNKNOWN HIP ACETABULAR LINERS
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWZ·December 12, 2019
MICROPLEX (MCS)
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code HCG·May 5, 2009
UNKNOWN HIP ACETABULAR LINERS
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWZ·December 12, 2019
UNKNOWN MALLORY-HEAD HIP
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·November 4, 2016
UNKNOWN M2A-MAGNUM HIP
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·November 4, 2016
UNKNOWN M2A-MAGNUM HIP
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·November 4, 2016
UNKNOWN KNEE
FDA Adverse Event
Injury
·BIOMET UK LTD·Product code NRA·May 27, 2015
ELECSYS 2010 RACK
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code DHA·April 5, 2010
UNKNOWN HIP ACETABULAR LINERS
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWZ·December 12, 2019