FDAFDA · Food and drugs·Recall number D-0909-2016
SUPER HERBS 350 mg, 30 capsules per bottle.
Published June 1, 2016 · Recall initiated: November 23, 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 - presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and/or phenolphthalein.
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- Super Herbs
- Distributor
- 9 consignees - only 9 bottles distributed
- Lot
- All lots
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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