14 results · 22ms · Sources: EU EUDAMED, US FDA

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FDA Adverse Event
Injury ·ABBOTT VASCULAR INC.·Product code MGB·July 8, 2024

COBAS 6000 C501 MODULE

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·March 26, 2013

POWER PRO AMBULANCE COT

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code INK·February 16, 2011

HIRES 90K

FDA Adverse Event
Malfunction ·ADVANCED BIONICS LLC·Product code MCM·March 24, 2008

ID NOW COVID-19 ASSAY

FDA Adverse Event
Injury ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·May 13, 2021

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FDA Adverse Event
Injury ·ABBOTT VASCULAR INC.·Product code MGB·June 12, 2024

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR·Product code MGB·July 25, 2022

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FDA Adverse Event
Injury ·ABBOTT VASCULAR INC.·Product code MGB·June 19, 2024

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FDA Adverse Event
Injury ·ABBOTT VASCULAR INC.·Product code MGB·June 19, 2024

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FDA Adverse Event
Injury ·ABBOTT VASCULAR INC.·Product code MGB·June 19, 2024

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FDA Adverse Event
Injury ·ABBOTT VASCULAR INC.·Product code MGB·June 19, 2024

ID NOW COVID-19 ASSAY

FDA Adverse Event
Injury ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·May 13, 2021

ID NOW COVID-19 ASSAY

FDA Adverse Event
Injury ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·May 13, 2021

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FDA Adverse Event
Injury ·ABBOTT VASCULAR INC.·Product code MGB·January 13, 2025