10 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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GORE® VIABAHN® ENDOPROSTHESIS WITH HEPARIN BIOACTIVE SURFACE
FDA Adverse Event
Malfunction
·W. L. GORE & ASSOCIATES, INC.·Product code PFV·July 14, 2021
UNICEL® DXC 600 PRO SYNCHRON® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·July 5, 2011
LIGAMAX-5MM ENDO CLIP APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 6, 2013
FLEXI-CUT DIRECTIONAL DEBULKING SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MCX·August 27, 2008
CONTOUR PLUS LINK 2.4
FDA Adverse Event
Malfunction
·ASCENSIA DIABETES CARE US INC.·Product code NBW·May 19, 2020
CONTOUR NEXT
FDA Adverse Event
Malfunction
·ASCENSIA DIABETES CARE US INC.·Product code NBW·February 24, 2020
CONTOUR PLUS LINK 2.4
FDA Adverse Event
Malfunction
·ASCENSIA DIABETES CARE US INC.·Product code NBW·August 1, 2019
CONTOUR PLUS LINK 2.4
FDA Adverse Event
Malfunction
·ASCENSIA DIABETES CARE US INC.·Product code NBW·August 1, 2019
CONTOUR PLUS LINK 2.4
FDA Adverse Event
Malfunction
·ASCENSIA DIABETES CARE US INC.·Product code NBW·August 1, 2019
GORE® VIABAHN® ENDOPROSTHESIS WITH HEPARIN BIOACTIVE SURFACE
FDA Adverse Event
Malfunction
·W. L. GORE & ASSOCIATES, INC.·Product code PFV·July 22, 2021