8 results
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42ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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BD MICROTAINER® MAP MICROTUBE FOR AUTOMATED PROCESS K2 EDTA 1.0 MG
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·August 24, 2021
VERIFLEX¿
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·January 10, 2013
NEXGEN LPS-FLEX GSF FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·April 3, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·March 25, 2011
INDURA
FDA Adverse Event
Injury
·RICE CREEK MANUFACTURING·Product code LKK·May 7, 2008
VERIFLEX (LIBERTE) CORONARY STENT DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code MAF·June 17, 2010
UNK BACTISEAL CATHETER
FDA Adverse Event
Injury
·Product code JXG·March 24, 2017
PDS PLUS VIO 20X45CM 0 S/A CTB-1 CR
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code NEW·October 2, 2024