402 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
VENA TECH VENA CAVA FILTER
FDA Adverse Event
Malfunction
·B. BRAUN VENA-TECH·Product code DTK·May 12, 1998
ELECSYS 2010
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·May 17, 2007
ANALYTICAL E MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LGD·June 3, 2007
INTEGRA 700
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·April 4, 2007
VENA TECH VENA CAVA FILTER
FDA Adverse Event
Malfunction
·B. BRAUN VENA-TECH·Product code DTK·April 30, 1998
ORTHO PROVUE
FDA Adverse Event
Malfunction
·MICRO TYPING SYSTEMS, INC.·Product code KSZ·November 2, 2009
SARS-COV-2 IGM
FDA Adverse Event
Malfunction
·ABBOTT IRELAND·Product code QKO·March 9, 2021
GLOVER, EXAMINING, LG, M, & SM.
FDA Adverse Event
Malfunction
·SPECTRUM LABORATORIES, INC.·Product code LYY·June 20, 1997
AEROSTAR RS 0100
FDA Adverse Event
Malfunction
·STACKHOUSE, INC.·Product code LGM·April 24, 1997
AEROSTAR RS 0100
FDA Adverse Event
Malfunction
·STACKHOUSE, INC.·Product code LGM·April 24, 1997
VANCOMYCIN
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LEH·June 25, 2019
GAMMA CLONE ANTI-D LGM-LGG (MONOCLONAL BLEND)
FDA Adverse Event
Malfunction
·IMMUCOR·Product code KSZ·May 26, 2006
VITROS IMMUNODIAGNOSTICS PRODUCTS AHBC IGM REAGENT PACK
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code LOM·February 1, 2008
UNKNOWN OPTEASE VENA CAVA FILTER
FDA Adverse Event
Malfunction
·CORDIS CORPORATION·Product code DTK·November 3, 2014
AXSYM TOTAL BHCG
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code JHI·August 16, 2007
PC-EDO
FDA Adverse Event
Malfunction
·HGM·Product code GEX·March 8, 2005
TOXOPLASMA 1GM
FDA Adverse Event
Malfunction
·SIGMA DIAGNOSTICS·Product code LGD·January 2, 2002
VANCOMYCIN 1GM
FDA Adverse Event
Malfunction
·HOSPIRA·Product code KPE·November 18, 2010
TOXOPLASMA 1GM
FDA Adverse Event
Malfunction
·SIGMA DIAGNOSTICS·Product code LGD·October 9, 2001
HGM PCC-EDO 2.5W
FDA Adverse Event
Malfunction
·HGM, INC.·Product code GFX·November 8, 1999