10 results
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26ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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ALERE DETERMINE HIV 1/2 AG/AB COMBO
FDA Adverse Event
Malfunction
·ALERE SCARBOROUGH INC.·Product code MZF·June 11, 2018
SURESTEP
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·December 18, 2000
ELECSYS FT3 III
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CDP·December 17, 2018
ELECSYS TSH ASSAY
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JLW·December 17, 2018
HUDSON DISP MANUAL RESUS,ADULT W/FLOW DIVERTER
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BTM·April 21, 2017
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013
ITREL 3
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·June 17, 2011
CROSSCATH SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·March 6, 2019
ENDOSKELETON® TCS
FDA Adverse Event
Malfunction
·TITAN SPINE, LLC·Product code OVE·March 29, 2017
CROSSCATH SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·June 20, 2019