CLASS I Food recall · Reported 15 Jun 2016 · FDA Enforcement Report

StemVitae Multivitamin recalled by Nuvi Global

Nuvi Global is recalling Nuvi Global StemVitae Multivitamin, distributed in 20 states. The recall was initiated on 19 Apr 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot #15556

Quantity recalled273 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-1431-2016
FDA event ID: 73937
Recalling firm: Nuvi Global, Rancho Cucamonga, CA
Brand: Nuvi Global
Classification: Class I
Status: Terminated
Recall initiated: 19 Apr 2016
FDA classified: 9 Jun 2016
Reported: 15 Jun 2016
Type: Voluntary: Firm initiated
Customers notified by: Telephone
Reason category: Undeclared Milk
Product category: Vitamins

Timeline

19 Apr 2016	Recall initiated by company
9 Jun 2016	Classified by FDA	+51 days
15 Jun 2016	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared whey protein which contains the allergens of milk and soy lecithin.

Product as listed by the FDA

Nuvi Global StemVitae Multivitamin 30oz.

Where it was distributed

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.

California Colorado Florida Iowa Idaho Illinois Indiana Maryland Minnesota Missouri Mississippi New Hampshire New Jersey Nevada New York Oklahoma South Carolina Texas Utah Washington

Questions about this recall

Is StemVitae Multivitamin recalled?

Yes. Nuvi Global recalled StemVitae Multivitamin on 19 Apr 2016. The recall is Class I and its status is Terminated. Recall number F-1431-2016.

Why was it recalled?

Undeclared whey protein which contains the allergens of milk and soy lecithin.

Which lots are affected?

Lot #15556

Where was it sold?

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.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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