12 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ALARIS® PUMP MODULE ADMINISTRATION SET
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·January 12, 2017
ALARIS® PUMP MODULE ADMINISTRATION SET
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·May 10, 2018
ALARIS PUMP MODULE ADMINISTRATION SET
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·November 13, 2017
FLEXTEND
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVN·October 10, 2012
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·December 3, 2013
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·August 2, 2010
ALARIS SECONDARY SET
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·November 14, 2016
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 10, 2013
ALARIS PUMP MODULE
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FRN·February 25, 2019
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·August 4, 2014
INFUSION ADAPTER C100-O
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code ONB·September 9, 2024
ALARIS PUMP MODULE
FDA Adverse Event
Injury
·CAREFUSION·Product code FRN·March 31, 2017