FDA recall record
Nuvi Global StemVitae Multivitamin 30oz.
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 February 9, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Nuvi Global StemVitae Multivitamin 30oz.
Reason
Undeclared whey protein which contains the allergens of milk and soy lecithin.
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.
Nuvi Global StemVitae Multivitamin 30oz.
Code information listed by FDA
Lot #15556
Distribution and firm information
Recalling firm listed by FDA: Nuvi Global Corporation
Firm location listed by FDA: Rancho Cucamonga, CA, United States
Distribution reported by FDA: U.S. distribution to the following; CA, CO, FL, IA, ID, IL, IN, MD, MN, MO, MS, NH, NJ, NV, NY, OK, SC, TX, UT, WA No foreign distribution.
Product quantity listed by FDA: 273 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.