38 results · 64ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

BRACCO DIAGNOSTIC INC 017345

FDA Adverse Event
Other ·BRACCO INJENEERING S.A.·Product code DXT·December 6, 2024

SYRINGE SINGLE 200CC INJECTOR SY

FDA Adverse Event
Malfunction ·BRACCO INJENEERING S.A.·Product code DXT·December 6, 2024

SYRINGE SINGLE 200CC INJECTOR SY

FDA Adverse Event
Malfunction ·BRACCO INJENEERING S.A.·Product code DXT·December 6, 2024

CT INJECTOR CEILING SUPPORT

FDA Adverse Event
Malfunction ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·December 13, 2019

ARTICULATING ARM OF EMPOWERCTA+

FDA Adverse Event
Malfunction ·BRACCO INJENEERING SA·Product code IZQ·February 28, 2018

CARDIOGEN-82®

FDA Adverse Event
Malfunction ·BRACCO DIAGNOSTIC INC.·Product code KPS·March 21, 2022

PROTOCOL TOUCH ADMINISTRATION SET

FDA Adverse Event
Injury ·BRACCO DIAGNOSTIC INC·Product code FCX·June 28, 2019

CT EXPRES

FDA Adverse Event
Injury ·BRACCO INJENEERING S.A.·Product code IZQ·April 21, 2026

PROTOCOL TOUCH ADMINISTRATION SET

FDA Adverse Event
Injury ·BRACCO DIAGNOSTICS INC·Product code FCX·June 28, 2019

FASTLOAD

FDA Adverse Event
Malfunction ·BRACCO DIAGNOSTICS INC.·Product code DXT·September 16, 2015

ADMINISTRATION SET FOLEY CATHETER

FDA Adverse Event
BRACCO DIAGNOSTICS, INC.·Product code FCX·December 11, 2014

PATIENT ADMIN SET FOR USE WITH THE CARDIOGEN-82 INFUSION SYS

FDA Adverse Event
Malfunction ·BRACCO DIAGNOSTICS INC·Product code FPA·October 1, 2014

PERCUCUT BONE BIOPSY NEEDLES

FDA Adverse Event
Malfunction ·BRACCO DIAGNOSTICS, INC·Product code KNW·November 9, 2009

PATIENT ADMIN. SET FOR USE WITH THE CARDIOGEN-82 INFUSION SYSTEM

FDA Adverse Event
Malfunction ·BRACCO DIAGNOSTICS INC.·Product code JAK·January 8, 2014

ISOVUE 370

FDA Adverse Event
Death ·BRACCO DIAGNOSTICS, INC.·Product code IZQ·September 29, 2004

SUPER XL ENEMA SYSTEM - 8925

FDA Adverse Event
Injury ·BRACCO DIAGNOSTICS INC.·Product code FGD·December 31, 2020

ISOVUE 300

FDA Adverse Event
Death ·BRACCO DIAGNOSTICS, INC.·Product code IZQ·September 29, 2004

PATIENT ADMIN. SET FOR USE WITH THE

FDA Adverse Event
Other ·BRACCO DIAGNOSTICS INC.·Product code FPK·August 25, 2014

ISOVUE-300

FDA Adverse Event
Malfunction ·BRACCO DIAGNOSTICS INC.·Product code FMF·April 19, 2004

ENEMA RING: FLUID COLLECTION DEVICE

FDA Adverse Event
Injury ·BRACCO DIAGNOSTICS INC·Product code FGD·October 31, 2023