FDAFDA · Food and drugs·Recall number D-600-2013
MAXILOSS Weight Advanced, 225 mg proprietary blend of herbs, supplied in 36 count capsules in Green & Blue Boxes, Formulated and distributed by Olaax Corp, Lakeland, FL
Published June 19, 2013 · Recall initiated: February 12, 2013
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 contains sibutramine, a previously approved FDA drug removed from the U.S. marketplace for safety reasons, making it an unapproved new drug.
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- OLAAX International
- Distributor
- Nationwide, Puerto Rico and Venezuela and Bolivia
- Lot
- All Lots
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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