9 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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INFUSE BONE GRAFT DEVICE (RHBMP-2)
FDA Adverse Event
MEDTRONIC INC.·Product code NEK·April 3, 2013
MAHURKAR MAXID 23 CM
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FJS·March 25, 2011
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Injury
·ROCHE DIAGNOSTICS·Product code LFR·May 7, 2008
VERIFLEX¿
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·January 10, 2013
VERIFLEX (LIBERTE) CORONARY STENT DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code MAF·June 17, 2010
STEALTHSTATION¿ S8 SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC NAVIGATION, INC·Product code HAW·July 25, 2023
ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY
FDA Adverse Event
Injury
·COOK INC·Product code MIH·June 30, 2017
ZENITH FLEX WITH SPIRAL-Z TECHNOLOGY AAA ENDOVASCULAR GRAFT ILIAC LEG
FDA Adverse Event
Injury
·COOK INC·Product code MIH·June 30, 2017
ZENITH AAA ENDOVASCULAR GRAFT ILIAC LEG
FDA Adverse Event
Injury
·COOK INC·Product code MIH·November 27, 2019