10 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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BARD® UNIVERSAL CATHETERIZATION TRAY
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code OHR·February 15, 2019
IMED IV PUMP
FDA Adverse Event
Injury
·IMED CORP.·Product code FRN·December 4, 1995
I-STAT ACT CELITE CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JBP·August 23, 2022
I-STAT ACT CELITE CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JBP·August 23, 2022
OPEN SPINE CLAMP DRIVER
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·April 24, 2014
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Injury
·EV3 NEUROVASCULAR·Product code OUT·October 3, 2012
ACCU-CHEK ACTIVE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBW·September 5, 2007
I-STAT ACT CELITE CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JBP·October 11, 2022
I-STAT ACT CELITE CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JBP·January 11, 2023
I-STAT ACT CELITE CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JBP·January 11, 2023