OLAAX International recalls MAXILOSS Weight Advanced, 225 mg proprietary blend of herbs, supplied in 36 count capsules in Green & Blue Boxes, Formul

Recalled June 19, 2013 · FDA recall D-600-2013 · OLAAX International

Hazard

Marketed Without an Approved NDA/ANDA: product contains sibutramine, a previously approved FDA drug removed from the U.S. marketplace for safety reasons, making it an unapproved new drug. · FDA Class I

Units

600 boxes

Sold at

Nationwide, Puerto Rico and Venezuela and Bolivia

Description

Marketed Without an Approved NDA/ANDA: product contains sibutramine, a previously approved FDA drug removed from the U.S. marketplace for safety reasons, making it an unapproved new drug.

Product

MAXILOSS Weight Advanced, 225 mg proprietary blend of herbs, supplied in 36 count capsules in Green & Blue Boxes, Formulated and distributed by Olaax Corp, Lakeland, FL

Manufacturer(s)

OLAAX International

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →