Detox Transforms recalls EDGE Amplified Weight Release capsules, 400 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, G

Recalled May 13, 2015 · FDA recall D-0977-2015 · Detox Transforms

Hazard

Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared phenolphthalein and fluoxetine, making EDGE an unapproved drug. · FDA Class I

Units

150 bottles

Sold at

WV who distributed Nationwide.

Description

Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared phenolphthalein and fluoxetine, making EDGE an unapproved drug.

Product

EDGE Amplified Weight Release capsules, 400 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00417 4.

Manufacturer(s)

Detox Transforms

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