10,000 results
·
90ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
AMS LGX700 KIT
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS INC·Product code FAE·May 27, 2016
ULTRAXX NEPHROSTOMY BALLOON AND SET
FDA Adverse Event
Injury
·COOK INC·Product code LJE·September 19, 2018
STOMAHESIVE PROTECTIVE POWDER
FDA Adverse Event
Malfunction
·CONVATEC·Product code EXE·November 3, 2006
SUR-FIT AUTOLOCK DH FLEXIBLE SKIN BARRIER
FDA Adverse Event
Malfunction
·CONVATEC·Product code EZR·November 3, 2006
ZEBRA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code EZB·June 5, 2025
NEPHROSTOMY SHEATHS AND DILATORS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code GCC·June 5, 2025
UNKNOWN GUIDEWIRE
FDA Adverse Event
Injury
·C.R. BARD INC. (COVINGTON) -1018233·Product code FAD·October 23, 2025
URETERO-RENO FIBERSCOPE
FDA Adverse Event
Injury
·AIZU OLYMPUS CO., LTD.·Product code FGB·October 6, 2023
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS, INC·Product code JAA·July 4, 2007
8015 ALARIS SYSTEM PC UNIT
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·November 17, 2020
SHOCKPULSE LITHOTRIPSY TRANSDUCER.
FDA Adverse Event
Malfunction
·GYRUS ACMI, INC.·Product code FEO·June 21, 2024
GE OEC 9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·August 4, 2008
NEPHROMAX
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code LJE·April 20, 2026
1.5MM LACTOSORB,100X100MM PNL
FDA Adverse Event
BIOMET MICROFIXATION·Product code HRS·May 20, 2013
1.5MM LACTOSORB,100X100MM PNL
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HRS·May 20, 2013
1.5MM LACTOSORB,100X100MM PNL
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HRS·July 19, 2012
FLUOROSCOPIC X-RAY
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS, INC·Product code JAA·December 5, 2007
CLINAC 600 CD
FDA Adverse Event
Malfunction
·Product code IYE·July 6, 2006
ULTRAXX NEPHROSTOMY BALLOON AND SET
FDA Adverse Event
Malfunction
·COOK INC·Product code LJE·November 9, 2018
NEPHROMAX
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code LJE·December 2, 2021