4,465 results · 36ms · Sources: EU EUDAMED, US FDA

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CURITY MONO-FLO 14FR WO/PVPI

FDA Adverse Event
Malfunction ·TYCO HEALTHCARE/KENDALL·Product code KOD·May 3, 2007

ZYNO MEDICAL Z-800 INFUSION PUMP SYSTEM

FDA Adverse Event
Malfunction ·ZYNO MEDICAL, LLC·Product code FRN·July 25, 2023

VELA VENTILATOR

FDA Adverse Event
Injury ·CAREFUSION, INC·Product code CBK·May 1, 2017

ZYNO MEDICAL Z-800 INFUSION PUMP SYSTEM

FDA Adverse Event
Malfunction ·ZYNO MEDICAL, LLC·Product code FRN·August 17, 2023

ZYNO MEDICAL Z-800 INFUSION PUMP SYSTEM

FDA Adverse Event
Malfunction ·ZYNO MEDICAL, LLC·Product code FRN·July 21, 2023

ZYNO MEDICAL Z-800 INFUSION PUMP SYSTEM

FDA Adverse Event
Malfunction ·ZYNO MEDICAL, LLC·Product code FRN·August 17, 2023

GORE TAG THORACIC ENDOPROSTHESIS

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code MIH·June 11, 2009

ZYNO MEDICAL Z-800 INFUSION PUMP SYSTEM

FDA Adverse Event
Malfunction ·ZYNO MEDICAL LLC·Product code FRN·August 15, 2023

HD AUTOCLAVABLE CAMERA HEAD

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FET·November 4, 2020

ZYNO MEDICAL Z-800 INFUSION PUMP SYSTEM

FDA Adverse Event
Malfunction ·ZYNO MEDICAL, LLC·Product code FRN·April 21, 2023

ALLURA XPER FD

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·October 7, 2024

TOSOH HLC-723G8 ANALYZER G8

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code LCP·March 20, 2018

ON-Z C-BLOC 400ML, 2/14ML/HR SAF

FDA Adverse Event
Malfunction ·I-FLOW, LLC·Product code MEB·June 16, 2014

ZYNO MEDICAL Z-800 INFUSION PUMP SYSTEM

FDA Adverse Event
Malfunction ·ZYNO MEDICAL, LLC·Product code FRN·April 10, 2023

VELE VENTILATOR DIAMOND SERIES

FDA Adverse Event
Injury ·CARFUSION·Product code ONZ·November 21, 2014

SV300 VENTILATOR

FDA Adverse Event
Death ·SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD·Product code ONZ·August 6, 2020

MECHANICAL VENTILATOR

FDA Adverse Event
Malfunction ·MAQUET MEDICAL SYSTEMS USA·Product code ONZ·April 12, 2017

INTRALASE FS3

FDA Adverse Event
Injury ·ABBOTT MEDICAL OPTICS·Product code HNO·December 7, 2016

KERATOME, AC-POWERED

FDA Adverse Event
Injury ·AMO MANUFACTURING USA, LLC·Product code HNO·March 19, 2021

AIA-900

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code KHO·April 2, 2018