E-United States, i- Ukuphathwa Kwezokudla Nezidakamizwa (i-FDA) ikhombe izehlakalo eziyi-127 zokuquleka kanye “nezinye izimpawu zemizwa” kulandela ukusetshenziswa kukagwayi we-elekthronikhi, okungaphezu kwamacala angama-35 inhlangano yaseMelika enawo. ibonwe ngo-Ephreli odlule.
UKUSOLWA NAPHEZU KUNGABIKHO KOKUXHUMANA OKUKHONSI...
Ekuqaleni kuka-April, i- Ukuphathwa Kwezokudla Nezidakamizwa (FDA) ubesevele ekhipha isexwayiso mayelana nezingozi ezingaba khona zokushunqamuka, ngemuva kokwenza lokho bahlonze amacala angama-35 okuquleka okuhlukahlukene okuhambisana ne-vaping. Ngaphandle kokuthi esimemezelweni esisha kuleli sonto, i-FDA ibuyekeza izibalo zayo kakhulu phezulu, futhi ikhombisa ukuthi isithole cishe 127 imibiko yokuquleka kanye "nezinye izimpawu zemizwa" ezenzeka phakathi kuka-2010 no-2019. Lawa macala ayi-127 afaka angama-35 akhonjwe yi-FDA ngo-Ephreli odlule.
Nakuba kungekho ukuxhumana okuphathekayo okungasungulwa phakathi komkhuba wokukhipha umoya kanye nalezi zinhlekelele, ukuqondana kubonakala kumangalisa kakhulu, ikakhulukazi njengoba izingozi ezihlobene nokusetshenziswa kukagwayi we-elekthronikhi zikhonjwa ezinye izinhlangano ngesikhathi esifanayo. Ukuze kuqoqwe idatha eyengeziwe ukuze kutholwe noma kungaxhunywanga phakathi komkhuba wokushunqisa kanye nalokhu kubanjwa kwesithuthwane, i-FDA imema wonke umuntu ukuthi akhulume nganoma yisiphi isigameko ebesingenzeka ngemva kokusetshenziswa kukagwayi we-elekthronikhi.
« Kubalulekile ukuthi ochwepheshe bezokunakekelwa kwempilo, abathengi, abazali, othisha, abanye abantu abadala abathintekile, kanye nentsha kanye nabantu abadala abasebasha banikeze i-FDA imininingwane enemininingwane nganoma yisiphi isigameko esibucayi, esedlule noma esizayo, kulandela ukusetshenziswa kwe-e-cigarette. Sizibophezele ekulandeleni lolu daba eduze kanye nokuthatha izinyathelo ezengeziwe ezidingekayo ukuze sivikele umphakathi, ikakhulukazi abantu abasha bezwe lakithi, ezingozini zikagwayi we-elekthronikhi neminye imikhiqizo kagwayi. » ememezelwe I-Ned Sharpless, isekela likakhomishana we-FDA.
