FDA recall record
Lipodrene With 25mg Ephedra Extract 100CT UPC 8 57084 00056 9
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
Product described in an FDA recall
Lipodrene With 25mg Ephedra Extract 100CT UPC 8 57084 00056 9
Reason
The firm was notified by the FDA that the product contains the unapproved food additive 1,4-dimethylamylamine (DMAA).
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.
Lipodrene With 25mg Ephedra Extract 100CT UPC 8 57084 00056 9
Code information listed by FDA
Lot # 001211197, Exp. 12/25
Distribution and firm information
Recalling firm listed by FDA: Hi Tech Pharmaceuticals
Firm location listed by FDA: Norcross, GA, United States
Distribution reported by FDA: The product was shipped to the following states: AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, ME, MI, MO, MS, MT, NC, NE, NE, NJ, NM, NV, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, VT, WA & WI.
Product quantity listed by FDA: 19,068/100 ct 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.