FDAJanuary 25, 2015drug

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Terminated

Brands named

detox transformsdetox

UPCs

852175004174

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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