3,394 results
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43ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
VITEK 2 SYSTEM
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LTW·March 24, 2008
VITEK 2 GP TEST KIT
FDA Adverse Event
Injury
·BIOMERIEUX, INC.·Product code LON·May 13, 2010
VITEK 2 GRAM-POSITIVE IDENTIFICATION TEST KIT
FDA Adverse Event
Injury
·BIOMERIEUX, INC·Product code LQL·July 21, 2015
VIRONOSTIKA HTLV I/II
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC·Product code MTP·May 1, 2002
BACT/ALERT MP CULTURE BOTTLES
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code JTA·June 25, 2008
VITEK® 2 ANC ID TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC·Product code JSP·June 1, 2017
BACT/ALERT BPA AND BPN CULTURE BOTTLES
FDA Adverse Event
Other
·BIOMERIEUX, INC.·Product code JTA·December 9, 2008
VIDAS SARS-COV-2 IGM
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code QKO·October 6, 2020
VITEK® 2 ANC TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC·Product code JSP·May 30, 2017
VITEK® 2 ANC TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC·Product code JSP·May 24, 2017
VITEK® 2 AST-GP67 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·December 5, 2019
VIDAS CMV LGG ASSAY
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LFZ·June 15, 2004
BACT/ALERT FA PLUS (PLASTIC) 100 BTLS - 410851
FDA Adverse Event
Malfunction
·BIOMÉRIEUX, INC.·Product code MDB·August 22, 2024
BTA3D CONTROL MODULE, INDUSTRY - 210148
FDA Adverse Event
Malfunction
·BIOMÉRIEUX, INC.·Product code MDB·November 24, 2021
BACT/ALERT® FN PLUS CULTURE BOTTLE
FDA Adverse Event
Malfunction
·BIOMERIEUX INC.·Product code MDB·August 17, 2018
VITROS IMMUNODIAGNOSTIC PRODUCTS HS TROPONIN I REAGENT PACK
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code MMI·May 4, 2026
VITEK® 2 ANC TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC·Product code JSP·June 12, 2017
BACT/ALERT MP BLOOD CULTURE BOTTLE
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code JTA·August 7, 2008
TOSOH HLC-723G8 ANALYZER G8
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code LCP·March 11, 2018
VIRONOSTIKA HIV-1 MICROELISA SYSTEM
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code MTP·December 21, 2006