9 results
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41ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
VARIPULSE¿ BI-DIRECTIONAL CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code QZI·May 21, 2026
VIKING M MOBILE LIFT
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FSA·February 20, 2026
FLO-GARD 6201 VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FRN·November 24, 2008
INTEGRITY AFX
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWP·September 8, 2011
INGENIO
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 22, 2013
TRUPULSE¿ GENERATOR
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code QZI·December 1, 2025
TRUPULSE¿ GENERATOR
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code QZI·April 21, 2026
DVR PEG SMOOTH 2.0MM X 26MM
FDA Adverse Event
Malfunction
·BIOMET TRAUMA·Product code LXT·July 7, 2017
DVR PEG SMOOTH 2.0MM X 18MM
FDA Adverse Event
Malfunction
·BIOMET TRAUMA·Product code LXT·July 7, 2017