Nuvi Global StemVitae Multivitamin recall
Recalled by Nuvi Global Corporation · Rancho Cucamonga, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Undeclared whey protein which contains the allergens of milk and soy lecithin.
Undeclared allergens: Milk Soy
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Nuvi Global StemVitae Multivitamin 30oz.
Quantity: 273 bottles
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot #15556
Where it was sold
California Colorado Florida Iowa Idaho Illinois Indiana Maryland Minnesota Missouri Mississippi New Hampshire New Jersey Nevada New York Oklahoma South Carolina Texas Utah Washington
FDA's distribution note: 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.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk, soy; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Nuvi Global Corporation
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 19, 2016
- In FDA report of
- Jun 15, 2016
- Terminated
- Feb 9, 2017
- FDA recall number
- F-1431-2016 · event 73937
- Official record
- FDA enforcement report search