Izindaba - I-FDA igunyaza amasampula okuhlolwa kokuxilonga ekhaya okokuqala kwe-COVID-19 ngaphandle kwencwadi kadokotela

I-Food and Drug Administration izolo igunyaze Ikhithi Yeqoqo Lasekhaya Lokuhlola I-Pixel COVID-19 ye-LabCorp ukuthi isetshenziswe abantu abadala ngaphandle kwencwadi kadokotela.I-FDA ibuyekeze futhi yakhipha kabusha ukugunyazwa kokusetshenziswa kwezimo eziphuthumayo kokuhlolwa ukuze kuvunyelwe umuntu ukuthi aqoqe isampula ye-nasal swab ekhaya futhi ayithumele kwa-LabCorp ukuze ihlolwe, ngemiphumela emihle noma engavumelekile ilethwa umhlinzeki wezempilo ngocingo kanye nemiphumela engemihle ilethwa nge-imeyili. noma ingosi ye-inthanethi.

“Nakuba amakhithi amaningi okuqoqwa kwasekhaya angabhalwa ngohlu lwemibuzo olulula oluku-inthanethi, le khithi esanda kugunyazwa yokuqoqwa kumthengi isusa leso sinyathelo enqubweni, ivumele noma ubani ukuthi aqoqe isampula yakhe futhi ayithumele elebhu ukuze icutshungulwe,” kusho uJeff. Shuren, MD, umqondisi we-FDA's Center for Devices and Radiological Health.