Super Herbs recalls SUPER HERBS 350 mg, 30 capsules per bottle.
Recalled June 1, 2016 · FDA recall D-0909-2016 · Super Herbs
Hazard
Marketed without an approved NDA/ANDA - presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and/or phenolphthalein. · FDA Class I
Units
9 bottles
Sold at
9 consignees - only 9 bottles distributed
Description
Marketed without an approved NDA/ANDA - presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and/or phenolphthalein.
Product
SUPER HERBS 350 mg, 30 capsules per bottle.
Manufacturer(s)
Super Herbs
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →