7 results
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34ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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ARROW PERITONEAL LAVAGE CATH KIT:8FR
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC.·Product code GBW·February 15, 2017
ARROW PERITONEAL LAVAGE CATH KIT:8FR
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC.·Product code GBW·February 15, 2017
GORE® VIABAHN® ENDOPROSTHESIS WITH HEPARIN BIOACTIVE SURFACE
FDA Adverse Event
Malfunction
·W. L. GORE & ASSOCIATES, INC.·Product code PFV·July 14, 2021
IN TOUCH ZU
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·May 24, 2013
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE INC.·Product code JPA·August 19, 2008
GORE® VIABAHN® ENDOPROSTHESIS WITH HEPARIN BIOACTIVE SURFACE
FDA Adverse Event
Malfunction
·W. L. GORE & ASSOCIATES, INC.·Product code PFV·July 22, 2021
HUDSON ET TUBE,HVT,8.0,NOVA PLUS
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BTR·March 1, 2016