8 results
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38ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BD VACUTAINER® CTAD BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·June 4, 2018
BD VACUTAINER® CTAD BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 31, 2018
BD VACUTAINER® CTAD BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 3, 2018
PROGRAMMABLE VALVE IN-LINE W/ SIPHONGUARD
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF·Product code JXG·June 30, 2014
UNKNOWN EXTERNAL NEUROSTIMULATOR
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LGW·January 8, 2013
ACCU-CHEK SPIRIT COMBO
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS INC·Product code LZG·November 10, 2010
TI MATRIXMANDIBLE PREFORMED RECON PL/SMALL/LEFT/2.5MM THK
FDA Adverse Event
Malfunction
·SYNTHES MEZZOVICO·Product code JEY·February 6, 2017
RIGIDFIX FEM 3.3MM S/T XPIN
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code HTY·January 22, 2019