FDA recall record
SYNEDREX, Powerful stimulant weight loss solution, 45 capsules (UPC 764779-224592). Brand: Metabolic Nutrition.
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of September 20, 2024. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
SYNEDREX, Powerful stimulant weight loss solution, 45 capsules (UPC 764779-224592). Brand: Metabolic Nutrition.
Reason
Products contain Picamilon and/or methylpentane citrate (DMBA), which are not recognized as a dietary ingredients
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
SYNEDREX, Powerful stimulant weight loss solution, 45 capsules (UPC 764779-224592). Brand: Metabolic Nutrition.
Code information listed by FDA
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).
Distribution and firm information
Recalling firm listed by FDA: IQ Formulations, LLC
Firm location listed by FDA: Sunrise, FL, United States
Distribution reported by FDA: Unknown
Product quantity listed by FDA: Approximately 67,113 bottles
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.