Bee Xtreme recalls Jenesis Dietary Supplement Capsules, 350 mg, 60 count bottles, Manufactured for Timeless Solutions, 1810 E Sahara Ave #1
Recalled October 19, 2016 · FDA recall D-0021-2017 · Bee Xtreme
Hazard
Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein · FDA Class I
Units
13 bottles
Sold at
Unknown
Description
Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein
Product
Jenesis Dietary Supplement Capsules, 350 mg, 60 count bottles, Manufactured for Timeless Solutions, 1810 E Sahara Ave #100, Las Vegas, Nevada 89104, distributed by BeeXtreme LLC, Punxsutawney PA
Manufacturer(s)
Bee Xtreme
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →