10 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
LS PRIM PLUMSET-SL PE-LINED
FDA Adverse Event
Malfunction
·ICU MEDICAL COSTA RICA LTD.·Product code FPA·December 13, 2021
COBAS EGFR MUTATION TEST
FDA Adverse Event
ROCHE MOLECULAR SYSTEMS, INC.·Product code OWD·January 29, 2014
SERVO-I
FDA Adverse Event
Malfunction
·MAQUET CRITICAL CARE AB·Product code CBK·June 3, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 5, 2011
RESERVOIR 3ML
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·October 7, 2014
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
COBAS EGFR MUTATION TEST
FDA Adverse Event
ROCHE MOLECULAR SYSTEMS·Product code OWD·January 14, 2015
PERCEVAL PLUS SUTRUELESS AORTIC HEART VALVE
FDA Adverse Event
Injury
·CORCYM S.R.L.·Product code LWR·January 12, 2025