7 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH INC.·Product code QJR·January 11, 2021
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·May 8, 2018
GRAFTMASTER RX CORONARY STENT GRAFT SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR·Product code MAF·December 15, 2021
SJM MECHANICAL HEART VALVE W/TEFLON CUFF
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, PUERTO RICO, INC. (CS)·Product code LWQ·March 15, 2013
GORE HYBRID VASCULAR GRAFT
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code DSY·February 28, 2011
VITROS IMMUNODIAGNOSTICS PRODUCTS ANTI-HCV REAGENT
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code MZO·August 15, 2014
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·May 22, 2018