10,000 results · 90ms · Sources: EU EUDAMED, US FDA

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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