FDA waxay si firfircoon ula socotaa nidaamka deegaanka ee khadka tooska ah ee alaabada been abuurka ah ee ay wadaan jilayaasha xun ee doonaya inay ka faa'iidaystaan ​​​​masiibada adduunka.Wakaaladdu waxay sheegtay inay heshay boqollaal badeecado COVID-19 ah oo been abuur ah, oo ay ku jiraan dawooyin, xirmooyinka baaritaanka, iyo PPE-da oo lagu iibiyay internetka iyadoo la sheegayo sheegashooyin aan la xaqiijin.Waxay la shaqaynaysaa suuqyada online-ka ah, diiwaan-geliyayaasha magaca domain-ka, soo-saarayaasha lacag-bixinta, iyo shabakadaha warbaahinta bulshada si ay meesha uga saaraan sheegashooyinka aan la xaqiijin ee goobahooda.

Ilaa hadda, FDA waxay soo saartay in ka badan 65 warqadood oo digniin ah.Xaaladaha qaarkood, FDA waxay raacday warqadaha digniinta ah iyadoo waydiisanaysa DOJ inay bilawdo dacwado sharci oo rasmi ah oo ka dhan ah soo saaraha alaabta.Qaybaha badeecadaha qaarkood, FDA waxay adeegsatay ogeysiisyada saxaafadeed si ay si wax ku ool ah u siiso digniin guud dhammaan soosaarayaasha meesha bannaan.Hoos waxaan ku taxnay dhammaan dadaallada dhaqangelinta ee FDA ay adeegsaneysay si ay isugu daydo in ay ka ilaaliso badeecadaha COVID-19 ee been abuurka ah suuqa.

FDA iyo FTC waxay soo direen waraaqahooda digniinta wareega koowaad saddex bilood ka hor.Hadda, FDA waxay soo saartay ugu yaraan 66 waraaqood oo digniin ah shirkadaha iibinaya alaabada been abuurka ah iyagoo sheeganaya inay ka hortagayaan, baarayaan, daaweynayaan, yareynayaan, ama daaweynayaan COVID-19.

Alaabooyinka waxaa ka mid ah (1) alaabada CBD, (2) kaabiska cuntada iyo fiitamiinnada, (3) saliidaha lagama maarmaanka ah, (4) alaabada dhirta, (5) alaabada homeopathic, (6) alaabada nadaafadda, (7) alaabada lagu calaamadeeyay inay ku jiraan koloriin dioxide. ama qalin qalin ah, iyo (8) kale.FDA waxay soo saartay arrin ku saabsan sheegashooyin suuqgeyneed oo kala duwan - oo u dhexeeya #coronavirus hashtags ilaa bayaanada lagu sameeyay daaqadaha soo booda.Shaxda hoose waxay taxaysaa warqadaha digniinta ee qaybta alaabta oo waxay tilmaamaysaa qaar ka mid ah weedhaha dhibka leh ee ay FDA aqoonsatay.Jaantuska tixraaca ahi waa inuu faa'iido u yeeshaa sidii loo go'aamin lahaa halka ay FDA diiradda saarayso dadaalladeeda dhaqangelineed marka ay timaado sheegashooyinka COVID-19.Xidhiidhada waraaqaha digniinta ayaa sidoo kale la bixiyaa alaab kasta.

Borotokoolka Coronavirus (Shaaha Lafaha Coronavirus, Ilaalinta Unugyada Coronavirus, Tincture Muhiimka ah ee Coronavirus, Nidaamka Difaaca ee Coronavirus, iyo Tincture Elderberry)

"Quicksilver Liposomal Vitamin C iyo Liposomal," "Jigsaw Magnesium oo leh SRT," iyo alaabada lagu calaamadeeyay inay ka kooban yihiin lacag

"Superblue Silver Immune Gargle," "SuperSilver Whitening Paste," "SuperSilver Wound Dressing Jeel" iyo "Superblue Fluoride Free cadayga"

HealthMax Nano-Silver Dareere, Silver Biotics Silver Lozenges oo leh Vitamin C, iyo Silver Biotics Silver Gel Ultimate Maqaarka & Daryeelka Jirka (wadar ahaan, "alaabtaada qalinka ah")

Silver, alaabta CBD, iodine, boqoshaada daawada, selenium, zinc, vitamin C, vitamin D3, astragalus, iyo elderberry

"China Oral Nosode," oo lagu sifeeyay "AN330 - TAAGEERADA CAAFIMAADKA CAAFIMAADKA EE CORONAA IYO/AMA INFEKARKA NAFKA FIRKA AH EE DA 'ASTA'

Warqadaha digniinta FDA waxay u bateen tallaabo sharci ugu yaraan laba xaaladood.Sidii aan horayba u soo sheegnay, FDA waxay uga digtay iibiyaha alaabada koloriin-dioxide inay alaabteeda ka saarto suuqa 48 saacadood gudahood.Ka dib markii iibiyaha "ay caddeeyeen in aysan dooneynin inay qaadaan tillaabo sax ah," DOJ waxay heshay amar xannibaad ku meel gaar ah oo ka dhan ah.

Sidoo kale, DOJ waxay heshay amar xannibaad ku meel gaar ah oo ka dhan ah iibiyaha alaabada qalinka ah ee kolloidal kaas oo, in kasta oo "ay ka saareen] bogaggoodii COVID-19 ee la xiriira in muddo ah, ...waxay dib u bilaabeen suuqgeyntooda alaabtooda qalinka ah si ay u daaweeyaan COVID-19 si sharciga waafaqsan.”

Labada xaaladoodba, FDA waxay muujisay inay jirto la'aan xog ku filan oo lagu dejiyo badbaadada iyo waxtarka alaabooyinka "isticmaalka kasta," iska daa in loo isticmaalo coronavirus-ga cusub.Wakaaladu waxay walaac ka muujisay in sheegashadan oo kale ay keeni karto in macaamiishu ay daahiyaan ama joojiyaan daawaynta ku haboon.In kasta oo ay siisay soosaarayaasha wax soo saarka fursad ay ku qaadaan tallaabo sax ah, waxay ugu dambeyntii raacday hanjabaadda tallaabo sharci ah.

FDA waxay sidoo kale adeegsatay ogeysiisyada saxaafadeed ee maalinlaha ah si ay ula xiriirto soosaarayaasha wax soo saarka COVID-19, gaar ahaan kuwa soo saara baaritaanka guriga iyo kuwa soo saara baaritaanka serology.

Mid ka mid ah ogeysiisyada noocaas ah, FDA waxay ka digtay inaysan oggolaanin wax tijaabo ah oo is-uruurin ah - in kasta oo ay jiraan mowjado tijaabooyin ah oo isku diyaarinaya inay ku dhacaan suuqa.Waxay dhawaan muujisay furfurnaan badan oo fikradda, inkastoo.Sidii aan horay u soo sheegnay, waxay siisay oggolaanshaha isticmaalka degdega ah (EUA) xirmada aruurinta guriga, xirmada guriga ee candhuufta ku saleysan, iyo xirmada guriga ee goonida ah.Waxay xitaa bilowday bixinta Tusaalaha Guriga ee Ururinta Molecular Diagnostic EUA Template si ay u sii taageerto horumarinta tijaabooyinka is-ururinta guriga.

Sidoo kale, FDA waxay daabacday dhowr ogeysiis saxaafadeed oo sidan oo kale ah oo sharraxaysa mawqifkeeda imtixaannada serology.Wakaaladu waxay hore u ilaalisay siyaasad dabacsan oo ku saabsan tijaabooyinka serology, ilaa badhtamihii Maarso, iyada oo u oggolaanaysa tijaabooyinka ka hortagga jirka ee ganacsiga in la suuq geeyo oo la isticmaalo iyada oo aan FDA EUA dib u eegin haddii ay raacaan shuruudaha qaarkood.Laakiin FDA ayaa cusboonaysiisay siyaasaddan bishii hore, wax yar ka dib guddi-hoosaadyada kongareeska ayaa ku dhaleeceeyay hay'adda "ku guuldareystay [booliisku]" suuqa tijaabada shaybaarka ee cudurka 'coronavirus'.

AFEEF: Sababtoo ah guud ahaan warka cusub, macluumaadka halkan lagu soo bandhigay waxaa laga yaabaa inaan lagu dabaqi karin xaaladaha oo dhan mana aha in lagu dhaqmo iyada oo aan la helin talo sharci oo gaar ah oo ku salaysan xaalado gaar ah.

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