536 results · 107ms · Sources: EU EUDAMED, US FDA

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ADVIA 2120I WITH DUAL ASPIRATE AUTOSAMPLER

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code GKZ·April 28, 2015

ADVIA 2120 WITH DUAL ASPIRATE AUTOSAMPLER

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code GKZ·April 20, 2015

UNICEL DXL800 ACCESS IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code JJE·December 14, 2011

COULTER LH 750 HEMATOLOGY ANALYZER

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·May 28, 2012

UNICEL® DXL 600 ACCESS® IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code JJE·June 25, 2012

ADVIA 1800

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·June 10, 2014

NEXGEN LEGACY LPS ARTICULAR SURFACE

FDA Adverse Event
Injury ·ZIMMER INC·Product code JWH·June 22, 2012

UNICEL® DXL 600 ACCESS® IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code JJE·May 8, 2012

ADVIA 2120I WITH SINGLE ASPIRATE AUTOSAMPLER

FDA Adverse Event
Malfunction ·SIMENES HEALTHCARE DIAGNOSTICS INC.·Product code GKZ·February 26, 2015

DIMENSION CLINICAL CHEMISTRY SYSTEM

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code MMI·February 6, 2009

COULTER LH 750 ANALYZER

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code LOQ·March 31, 2011

UNICEL DXL800 ACCESS IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code JJE·August 9, 2012

COULTER LH 500 HEMATOLOGY ANALYZER

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·July 24, 2012

COULTER® LH 500 HEMATOLOGY ANALYZER

FDA Adverse Event
Malfunction ·BECKMAN COULTER·Product code GKZ·January 29, 2014

ASPIRE CRISTALLE

FDA Adverse Event
Injury ·FUJIFILM CORPORATION·Product code OTE·July 10, 2019

VITROS ECI IMMUNODIAGNOSTIC SYSTEM

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KHO·January 6, 2010

WHITESTAR SIGNATURE PRO

FDA Adverse Event
Injury ·AMO MANUFACTURING USA, LLC·Product code HQC·August 29, 2024

SYNCHRON LXI 725 SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code JLB·May 30, 2012

INTROCAN SAFETY®

FDA Adverse Event
Malfunction ·B. BRAUN MELSUNGEN AG·Product code FOZ·June 14, 2019

UNICEL® DXI 800 ACCESS® IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code JJE·June 16, 2011