10,000 results
·
168ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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BECTON DICKINSON & CO
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO·Product code FMI·February 13, 2004
BECTON, DICKINSON AND CO
FDA Adverse Event
Malfunction
·*·Product code FMF·January 30, 2004
BECTON DICKINSON & CO
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMF·January 11, 2002
BECTON DICKINSON & CO
FDA Adverse Event
BECTON DICKONSON & CO.·Product code FMF·July 25, 2000
BECTON DICKINSON AND CO.
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMF·March 13, 2001
BECTON DICKINSON & CO.
FDA Adverse Event
Malfunction
·BECTON DICKINSTON & CO·Product code KZH·July 21, 1994
BECTON DICKINSON & CO
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO.·Product code FMI·April 30, 1998
BECTON, DICKINSON & CO.
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·March 16, 2009
BECTON DICKINSON AND CO.
FDA Adverse Event
Injury
·Product code FMI·February 14, 2019
BECTON DICKINSON & CO
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO·Product code FMF·June 8, 2001
BECTON DICKINSON & CO
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO.·Product code FMI·November 20, 1998
BECTON DICKINSON AND CO.
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO.·Product code FMF·December 4, 1998
BECTON DICKINSON & CO
FDA Adverse Event
Malfunction
·*·Product code FMF·November 14, 2002
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code OOI·October 30, 2023
BD VACUTAINER® SST¿ BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·April 30, 2018
BECTON, DICKINSON & CO. (SPARKS)
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·February 20, 2023
BECTON, DICKINSON & CO. KERRISON
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. / CAREFUSION 2200, INC.·Product code HAE·December 31, 2020
BD -BECTON DICKINSON AND CO.
FDA Adverse Event
Malfunction
·BD·Product code FMF·May 17, 2006
BECTON DICKINSON & CO. SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO.·Product code FMF·July 26, 2001
BD ULTRA FINE¿ PEN NEEDLES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND CO.·Product code FMI·April 8, 2019