Reported May 13, 2015 · Terminated
EDGE Amplified Weight Release capsules, 400 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227,…
Detox Transforms
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Detox Transforms · 1027 Us Highway 70 W · Garner, NC · 27529-2501
Is this the product you have?
EDGE Amplified Weight Release capsules400 mg60-count bottleDeveloped by Signature1027 Highway 70 WSuite 227GarnerNC 27529UPC 8 52175 00417 4
- Lot codes and dates
- LotsALL
- Amount recalled
- 150 bottles
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
- Nationwide
- WV
Why it was recalled
Stop using this product now
Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared phenolphthalein and fluoxetine, making EDGE an unapproved drug.
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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