IQ Formulations Synedrex Recall

Products contain Picamilon and/or methylpentane citrate (DMBA), which are not recognized as a dietary ingredients

SYNEDREX, Powerful stimulant weight loss solution, 45 capsules (UPC 764779-224592). Brand: Metabolic Nutrition.

Lots: 1607404 (Exp 03/2019), 1607405 (Exp 03/2019), 1607406 (Exp 03/2019), 1607407 (Exp 03/2019), 1607501 (Exp 03/2019), 1607502 (Exp 03/2019), 1607503 (Exp 03/2019), 1607504 (Exp 03/2019), 1607505 (Exp 03/2019), 1607506 (Exp 03/2019), 1607510 (Exp 03/2019), 1607511 (Exp 03/2019), 1607512 (Exp 03/2019) 1607602 (Exp 03/2019), 1607603 (Exp 03/2019) 1607604 (Exp 03/2019), 1607605 (Exp 03/2019), 1607606 (Exp 03/2019), 1607607 (Exp 03/2019), 1607608 (Exp 03/2019), 1607609 (Exp 03/2019), 1607610 (Exp 03/2019), 1607611 (Exp 03/2019), 1607612 (Exp 03/2019), 1607613 (Exp 03/2019), 1607614 (Exp 03/2019), 1609601 (Exp 05/2019), 1609602 (Exp 05/2019), 1609603 (Exp 05/2019), 1609604 (Exp 05/2019), 1609605 (Exp 05/2019), 1609701 (Exp 05/2019), 1609702 (Exp 05/2019), 1609703 (Exp 05/2019), 1609704 (Exp 05/2019), 1609705 (Exp 05/2019), 1609706 (Exp 05/2019), 1609707 (Exp 05/2019), 1609708 (Exp 05/2019), 1609709 (Exp 05/2019), 1609801 (Exp 05/2019), 1609802 (Exp 05/2019), 1617205 (Exp 06/2019), 1617206 (Exp 06/2019), 1617208 (Exp 06/2019), 1617209 (Exp 06/2019), 1619001 (Exp 07/2019), 1619002 (Exp 07/2019), 1619003 (Exp 07/2019), 1619004 (Exp 07/2019), 1619006 (Exp 07/2019), 1619007 (Exp 07/2019), 1619008 (Exp 07/2019), 1619301 (Exp 07/2019), 1619302 (Exp 07/2019), 1619303 (Exp 07/2019), 1619304 (Exp 07/2019), 1619305 (Exp 07/2019), 1619306 (Exp 07/2019), 1619504 (Exp 07/2019), 1619505 (Exp 07/2019), 1619506 (Exp 07/2019), 1619507 (Exp 07/2019).

Unknown

• Compare the brand, size, and lot/UPC codes on your package with the codes above.
• If it matches, don't eat it. Return it to the store for a refund or throw it away.
• Wash surfaces and containers that touched the product.
• If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall number

F-1345-2017

Classification

Class II

Status

Terminated

Recall initiated

Aug 16, 2016

FDA report date

Feb 1, 2017

Quantity

Approximately 67,113 bottles

Recall type

Voluntary: Firm initiated

Recalling firm

IQ Formulations, LLC