10,000 results · 89ms · Sources: EU EUDAMED, US FDA

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CANTEL MEDIVATOR - ADVANTAGE PLUS ADV

FDA Adverse Event
Malfunction ·MEDIVATORS INC.·Product code FEB·March 10, 2023

CANTEL MEDIVATOR - ADVANTAGE PLUS ADV

FDA Adverse Event
Malfunction ·MEDIVATORS INC.·Product code FEB·March 10, 2023

CANTEL MEDIVATOR - ADVANTAGE PLUS ADV

FDA Adverse Event
Malfunction ·MEDIVATORS INC.·Product code FEB·March 10, 2023

ARC ENDOCUFF

FDA Adverse Event
Injury ·BODDINGTONS PLASTICS LTD.·Product code FED·October 18, 2013

ARCTIC SUN® TEMPERATURE MANAGEMENT SYSTEM, ARCTICGEL¿ PADS

FDA Adverse Event
Malfunction ·MEDIVANCE, INC.·Product code DWJ·July 9, 2025

DSD-201

FDA Adverse Event
Injury ·MEDIVATORS·Product code FEB·December 19, 2018

EVIS EXERA II COLONOVIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·August 1, 2023

MEDIVATORS ENDO CARRY-ON PROCEDURE KIT

FDA Adverse Event
Malfunction ·MEDIVATORS·Product code OCX·July 23, 2018

SYSTEM 83 PLUS

FDA Adverse Event
Death ·CUSTOM ULTRASONICS INC.·Product code FEB·March 24, 2016

EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDS·July 15, 2022

EVIS EXERA III DUODENOVIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDT·July 15, 2022

EVIS EXERA III COLONOVIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·July 14, 2022

POTASSIUM AND CALCIUM ELECTROLYTE POWDER PACKETS

FDA Adverse Event
Other ·EDLAW PHARMACEUTICALS, INC.·Product code KPO·November 1, 2023

ACID DIALYSATE BATH

FDA Adverse Event
Other ·MEDIVATORS, INC.·Product code FKQ·November 1, 2023

ION

FDA Adverse Event
Injury ·INTUITIVE SURGICAL, INC·Product code EOQ·May 7, 2026

EVIS EXERA II COLONOVIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·July 13, 2022

DIALYSATE SOLUTION

FDA Adverse Event
Other ·MEDIVATORS INC.·Product code KDI·January 2, 2024

FUJINON

FDA Adverse Event
Malfunction ·FUJINON, INC.·Product code EOQ·March 25, 2013

FUJINON

FDA Adverse Event
Malfunction ·FUJINON, INC.·Product code EOQ·March 25, 2013

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·June 5, 2023