11 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
T:SLIM G4 SYSTEM
FDA Adverse Event
Injury
·TANDEM DIABETES CARE·Product code OYC·December 19, 2016
CARTIVA
FDA Adverse Event
Injury
·CARTIVA, INC·Product code PNW·July 21, 2020
THE HEART LASER CO2 TMR SYSTEM (P950015)
FDA Adverse Event
Injury
·NOVADAQ TECHNOLOGIES,=INC.·Product code MNO·September 8, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 7, 2014
DEMI PLUS
FDA Adverse Event
Injury
·KERR CORPORATION·Product code EBZ·July 5, 2011
MBT CEM TIBIAL TRAY SZ2.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS·Product code NJL·June 6, 2013
CARTIVA DEVICE 10MM T20-0329
FDA Adverse Event
Injury
·CARTIVA, INC·Product code PNW·April 23, 2021
PERCEVAL PLUS SUTURELESS AORTIC HEART VALVE
FDA Adverse Event
Death
·CORCYM S.R.L.·Product code LWR·April 10, 2025
PERCEVAL PLUS SUTRUELESS AORTIC HEART VALVE
FDA Adverse Event
Injury
·CORCYM S.R.L.·Product code LWR·February 25, 2025
PERCEVAL PLUS SUTURELESS AORTIC HEART VALVE
FDA Adverse Event
Malfunction
·CORCYM S.R.L.·Product code LWR·March 27, 2025
PERCEVAL PLUS SUTRUELESS AORTIC HEART VALVE
FDA Adverse Event
Injury
·CORCYM S.R.L.·Product code LWR·January 12, 2025