10 results
·
37ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
SAMPLE CUPS, 0.5 ML
FDA Adverse Event
BECKMAN COULTER, INC.·Product code NNI·October 6, 2011
BD SYRINGE 5ML LL TIP BULK CONVENIENCE PAK
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMF·December 20, 2019
SYRINGE 5ML LL TIP BULK CONVENIENCE PAK
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMF·December 9, 2019
SYRINGE 5ML LL TIP BULK CONVENIENCE PAK
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMF·December 23, 2019
SYRINGE 5ML LL TIP BULK CONVENIENCE PAK
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMF·December 27, 2019
SAMPLE CUPS, 0.5 ML
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code NNI·January 12, 2012
OPTIFLUX 180NRE DIALYZER FINISHED ASSY.
FDA Adverse Event
Malfunction
·OGDEN MANUFACTURING·Product code KDI·April 4, 2013
CORE IMPACTION DRILL
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·March 30, 2011
VITALITY VR
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008
DUO FLUID CART
FDA Adverse Event
Malfunction
·DORNOCH·Product code JCX·June 4, 2020