9 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BD VACUTAINER® 21 G X 1.5 IN. MULTI SAMPLE BLOOD COLLECTION NEEDLE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code FMI·November 30, 2017
SINAI HSP BALTIMORE MD 1
FDA Adverse Event
Other
·SORIN GROUP USA, INC.·Product code DTZ·July 6, 2011
LAKELAND REG LAKELAND FL 1
FDA Adverse Event
Other
·SORIN GROUP USA, INC.·Product code DWF·May 3, 2010
WA ADVENT TAKOMA PARK MD 1
FDA Adverse Event
Other
·SORIN GROUP USA, INC.·Product code DTZ·November 22, 2011
IOWA METH DES MOINES IA1
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code DTZ·March 7, 2011
COULTER® LH 500 HEMATOLOGY INSTRUMENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·May 3, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·September 16, 2014
UNKNOWN
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·May 5, 2011
METRX SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·June 10, 2024