5,638 results
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51ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
HOSPIRA INC.
FDA Adverse Event
Other
·HOSPIRA, INC.·Product code FRN·August 25, 2004
HOSPIRA INC
FDA Adverse Event
Injury
·*·Product code DRS·December 12, 2006
HOSPIRA, INC.
FDA Adverse Event
Death
·HOSPIRA, INC.·Product code FPA·December 19, 2006
LIFESHIELD TKO ANTI REFLUX VALVE
FDA Adverse Event
Malfunction
·HOSPIRA, INC.·Product code FPA·January 31, 2011
PERIFIX
FDA Adverse Event
Other
·B. BRAUN MEDICAL, INC.·Product code CAZ·February 22, 2007
PERIFIX
FDA Adverse Event
Other
·B. BRAUN MEDICAL, INC.·Product code CAZ·July 1, 2008
MICROCLACE MED INC - HOSPIRA
FDA Adverse Event
Malfunction
·Product code FPA·July 23, 2010
PENCAN SPINAL NEEDLE TRAY
FDA Adverse Event
Other
·B. BRAUN MEDICAL, INC.·Product code BSP·October 2, 2008
PORTEX
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC·Product code BSO·November 18, 2010
SPINOCAN SPINAL NEEDLE TRAY
FDA Adverse Event
Other
·B. BRAUN MEDICAL, INC.·Product code BSP·September 18, 2008
SAPPHIRE INFUSION PUMP
FDA Adverse Event
Malfunction
·Q CORE MEDICAL LTD.·Product code FRN·December 15, 2016
PREFILLED SYRINGE WITH LUER LOCK 0.5 ML
FDA Adverse Event
Malfunction
·HOSPIRA, INC.·Product code FMF·February 19, 2015
STERILE EMPTY VIAL AND INJECTOR 30ML
FDA Adverse Event
Injury
·HOSPIRA, INC.·Product code MEA·April 16, 2015
GLASS NEEDLES, 30ML SINGLE USE
FDA Adverse Event
Other
·HOSPIRA, INC.·Product code FMI·June 29, 2015
SAPPHIRE INFUSION PUMP- ENGLISH
FDA Adverse Event
Malfunction
·Q CORE MEDICAL LTD.·Product code FRN·January 15, 2017
SEE SECTION H10
FDA Adverse Event
Malfunction
·ICU MEDICAL COSTA RICA LTD.·Product code FPA·May 19, 2023
SAPPHIRE M.T INFUSION PUMP- US
FDA Adverse Event
Malfunction
·Q CORE MEDICAL LTD.·Product code FRN·November 17, 2016
ADD-A-NEEDLE SPINAL ANESTHESIA TRAY
FDA Adverse Event
Malfunction
·HOSPIRA, INC.·Product code CAZ·January 16, 2008
DOUBLE CONNECTOR 12009
FDA Adverse Event
Malfunction
·ICU MEDICAL/HOSPIRA·Product code FPA·January 21, 2016
SAPPHIRE M.T INFUSION PUMP - FRENCH
FDA Adverse Event
Malfunction
·Q CORE MEDICAL LTD.·Product code FRN·November 13, 2016