Nuvi Global StemVitae Multivitamin 30oz.

Nuvi Global Corporation recalled Nuvi Global in a Class I action — the FDA's most serious tier, reserved for products with a reasonable probability of causing serious health consequences or death on Apr 19, 2016.

The FDA listed the reason as an undeclared allergen: "Undeclared whey protein which contains the allergens of milk and soy lecithin." Allergen mislabeling is the leading cause of U.S. food recalls, because a missing declaration can trigger a reaction in someone who reads the label and believes the product is safe.

The product reached multiple states, recorded by the FDA as "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." A multi-state footprint means the same lot can surface in households far from the producer. The recalling firm is based in Rancho Cucamonga, CA. The recall covers 273 bottles of product. The FDA has Terminated this recall (first reported Jun 15, 2016), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.