FDA imaletsa Zinthu ziwiri za Vuse Brand Mint Flavored Vaping Products

Pa Januware 24, 2023, US Food and Drug Administration (FDA) idapereka Marketing Denial Order (MDO) yamitundu iwiri ya timbewu ta Vuse.e-fodyamankhwala ogulitsidwa ndi RJ Reynolds Vapor, wothandizira wa British American Fodya.

Zogulitsa ziwiri zomwe zaletsedwa kugulitsa ndi Vuse Vibe Tank Menthol 3.0% ndi Vuse CiroKatirijiMenthol 1.5%.Kampaniyo siyiloledwa kugulitsa kapena kugawa zinthu ku US, kapena atha kukhala pachiwopsezo cha FDA.Makampani angathe, komabe, kutumizanso pempholo kapena kutumiza pulogalamu yatsopano kuti athetse vuto lazinthu zomwe zili ndi dongosolo loletsa kutsatsa.

Uwu ndi mlandu wachiwiri woletsa fodya wa e-fodya wa kukoma uku pambuyo poti a FDA adapereka lamulo lokana kutsatsa kwa chinthu chokometsedwa cha Logic Technology Development, kampani ya Japan Tobacco International, mu Okutobala chaka chatha.

A FDA ati kugwiritsa ntchito mankhwalawa sikunapereke umboni wokwanira wasayansi wosonyeza kuti phindu lomwe lingakhalepo kwa osuta achikulire limaposa kuopsa kwa kugwiritsa ntchito achinyamata.

A FDA adawona kuti umboni womwe ulipo ukuwonetsa kuti si fodya wokometsedwae-ndudu, kuphatikizapo menthol flavorede-ndudu, "zoopsa zomwe zikudziwika komanso zoopsa zomwe achinyamata amakopeka nazo, kuwatenga, ndi kuwagwiritsa ntchito."Mosiyana ndi zimenezi, deta imasonyeza kuti e-fodya ya e-fodya alibe chidwi chofanana ndi achinyamata ndipo motero samakhala ndi chiopsezo chofanana.

Poyankha, Fodya waku Britain waku America adawonetsa kukhumudwa ndi lingaliro la FDA ndipo adati Reynolds apempha nthawi yomweyo kuyimitsa kukakamira ndipo afunafuna njira zina zoyenera kulola Vuse kuti apitilize kupereka zinthu zake popanda kusokonezedwa.

"Timakhulupirira kuti mankhwala otsekemera a menthol ndi ofunika kwambiri kuti athandize osuta achikulire kuti asakhale ndi ndudu zoyaka.Lingaliro la FDA, ngati liloledwa kuti liyambe kugwira ntchito, livulaza m'malo mopindulitsa thanzi la anthu, "atero mneneri wa BAT.Reynolds achita apilo lamulo loletsa kutsatsa la FDA, ndipo khothi la US lavomereza kuti chiletsocho chiyimitsidwe.