Product Detail

Product Description 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

Recall Number D-600-2013

Classification Class I

Code Info All Lots

Product Distributed Qty 600 boxes

Reason For Recall 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.

Event Detail

Event Id 64409

Product Type Drugs

Status Ongoing

Recalling Firm

OLAAX International
City Bartow
State FL
Country US

Voluntary / Mandated Voluntary: Firm Initiated

Recall Initiation Date 2013-02-12

Initial Firm Notification of Consignee or Public Telephone

Distribution Pattern Nationwide, Puerto Rico and Venezuela and Bolivia