EDGE Amplified Weight Release capsules recall
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…
Why was EDGE Amplified Weight Release capsules recalled?
Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared phenolphthalein and fluoxetine, making EDGE an unapproved drug.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lots: ALL
- 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…
- Recalling firm
- Detox Transforms
- Quantity
- 150 bottles
- Distribution
- WV who distributed Nationwide.
- Recall date
- May 13, 2015
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)