12 results
·
31ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
FLEXTEND IS-1 BI POSITIVE FIX
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code DTB·May 7, 2004
SYMPHONY
FDA Adverse Event
Injury
·SORIN CRM·Product code NVZ·July 12, 2017
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 12, 2024
MOSAIC AORTIC BIOPROSTHETIC HEART VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code LWR·September 7, 2017
CONTAK RENEWAL TR
FDA Adverse Event
Death
·CLONMEL·Product code NIK·October 17, 2008
RECAP MAGNUM SHELL
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWA·August 5, 2011
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 2, 2013
GASTROINTESTINAL VIDEOSCOPE
FDA Adverse Event
Malfunction
·AIZU OLYMPUS CO., LTD.·Product code FDS·October 21, 2022
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·October 11, 2017
BD Q-SYTE¿ EXTENSION SET MICRO BORE
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·October 5, 2018
BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·November 9, 2018
BD¿ Q-SYTE CLOSED LUER ACCESS DEVICE
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·December 11, 2018