32 results · 20ms · Sources: EU EUDAMED, US FDA

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ARCHITECT C16000

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code JJE·January 6, 2021

ARCHITECT C16000 SYSTEM

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES (IRVING IA/CC)·Product code JJE·March 19, 2020

ARCHITECT C4000 ANALYZER

FDA Adverse Event
Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·March 11, 2019

ARCHITECT C16000

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code JJE·June 14, 2021

ARCHITECT C4000

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code JJE·July 23, 2024

ARCHITECT C16000 SYSTEM

FDA Adverse Event
Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·July 16, 2019

ARCHITECT C16000 SYSTEM

FDA Adverse Event
Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·July 15, 2019

ARCHITECT C16000

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code JJE·February 9, 2022

ARCHITECT C8000 PROCESSING MODULE

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES (IRVING IA/CC)·Product code JJE·April 28, 2020

ARCHITECT C16000

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code JJE·April 17, 2023

ARCHITECT C4000 ANALYZER

FDA Adverse Event
Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·March 24, 2019

ARCHITECT C8000 SYSTEM

FDA Adverse Event
Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·April 26, 2019

ENDOTAK RELIANCE

FDA Adverse Event
Malfunction ·CPI - DEL CARIBE·Product code LWS·July 1, 2014

ARCHITECT C8000

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code JJE·March 14, 2022

ARCHITECT C4000

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code JJE·July 20, 2022

ARCHITECT C4000 ANALYZER

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES (IRVING IA/CC)·Product code JJE·August 21, 2020

ARCHITECT C16000 SYSTEM

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES (IRVING IA/CC)·Product code JJE·September 9, 2020

ARCHITECT C16000

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code JJE·September 8, 2021

1628664-2016-00231

FDA Adverse Event
Malfunction ·September 9, 2016

1628664-2016-00224

FDA Adverse Event
Malfunction ·September 1, 2016