9 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BLOOD GROUPING REAGENT ANTI-A (ABO1)
FDA Adverse Event
Malfunction
·BIO-RAD MED DIAGNOSTICS GMBH·Product code KSF·January 17, 2011
BLOOD GROUPING REAGENT ANTI-A (ABO1)
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code KSZ·January 24, 2011
VIDAS® RUB IGG II
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code LFX·September 10, 2019
BLOOD GROUPING REAGENT ANTI-A (ABO1)
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code KSZ·December 16, 2010
ENDO RETRACT II 10MM INSTRUMENT
FDA Adverse Event
Malfunction
·COVIDIEN FORMERLY USSC PUERTO RICO, INC.·Product code GAD·June 26, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 14, 2013
OT ULTRAMINI METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·February 28, 2011
VITROS XT 7600 INTEGRATED SYSTEM
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code JJE·February 5, 2026
VIDAS® BRAHAMS PROCALCITONIN
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code PRI·September 16, 2019