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FDAFDA · Food and drugs·Recall number D-0981-2015

iNSANE Bee Pollen capsules, 200 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00408 2.

Published May 13, 2015 · Recall initiated: January 25, 2015

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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

What to do

Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Recall details

Manufacturer
Detox Transforms
Distributor
WV who distributed Nationwide.
Lot
Lot: 0000:02, Exp 06/20/17
Risk classification
Class I
Area (FDA)
drug
Country
United States

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