23 results
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34ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
ENDOWRIST
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·March 6, 2026
VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I REAGENT PACK
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code MMI·May 24, 2007
VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I REAGENT PACK
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code MMI·May 24, 2007
NDI PASSIVE SPHERES
FDA Adverse Event
Malfunction
·NORTHERN DIGITAL, INC.·Product code HAW·July 11, 2014
DIMENSION(R) CLINICAL CHEMISTRY SYSTEM
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code MMI·March 5, 2012
PASADENA BAYSHORE HSP TX 1
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code DTZ·September 19, 2008
PASADENA BAYSHORE HSP TX 1
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code DTZ·September 19, 2008
ADVIA 560 HEMATOLOGY SYSTEM
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code GKZ·February 19, 2016
ENDOWRIST
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·January 29, 2026
RLV 2100B VACUUM RELIEF VALVE
FDA Adverse Event
Malfunction
·QUEST MEDICAL, INC.·Product code DWD·June 25, 2015
RLV 2100B VACUUM RELIEF VALVE
FDA Adverse Event
Malfunction
·QUEST MEDICAL, INC.·Product code DWD·June 25, 2015
RLV 2100B VACUUM RELIEF VALVE
FDA Adverse Event
Malfunction
·QUEST MEDICAL, INC.·Product code DWD·June 25, 2015
ENDOWRIST
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·August 22, 2024
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·May 1, 2012
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·May 1, 2012
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·May 1, 2012
SAV-ON ONE STEP PREGNANCY TEST
FDA Adverse Event
Malfunction
·PRINCETON BIOMEDITECH CORPORATON·Product code LCX·August 15, 1997
HERCEPTEST KIT
FDA Adverse Event
Malfunction
·DAKO CORP.·Product code LIJ·December 3, 1998
FENESTRATED, POLYAXIAL SCREW; SIZE 6.5X45 MM
FDA Adverse Event
Malfunction
·K2M, INC.·Product code NKB·September 18, 2019
TECNIS CL IOL
FDA Adverse Event
Malfunction
·AMO PUERTO RICO MFG. INC.·Product code HQL·September 10, 2021