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RECALL RECORD — CLASS IRecall closedF-1431-2016/FDA enforcement
Nuvi Global Corporation·Food·Apr 19, 2016

Nuvi Global Stemvitae Multivitamin 30oz

What you need to know

Class I

  • What happened

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

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall closed · classified by the FDACA, CO, FL, IA +16 moreMore food

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Product identification

Source: FDA FOOD

Brand nameNuvi Global Corporation
Recalling firmNuvi Global CorporationRancho Cucamonga, CA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot #15556
Distribution area
CACOFLIAIDILINMDMNMOMSNHNJNVNYOKSCTXUTWA

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.

United States

Quantity affected273 bottles
Recall initiationFDA report date: June 15, 2016
FDA recall numberF-1431-2016

Beyond the headline

The recall, in context

Nuvi Global Corporation initiated this food recall on April 19, 2016. The FDA enforcement report states: Undeclared whey protein which contains the allergens of milk and soy lecithin. The FDA report lists distribution 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.

The FDA enforcement report describes the reason as: Undeclared whey protein which contains the allergens of milk and soy lecithin.

Nuvi Global Stemvitae Multivitamin 30oz was made or distributed by Nuvi Global Corporation in Rancho Cucamonga, CA, United States. This page reflects FDA report F-1431-2016, dated June 15, 2016.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared milk

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a milk allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed cow's milk allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a milk allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Nuvi Global Stemvitae Multivitamin 30oz recall?

Nuvi Global Corporation recalled Nuvi Global Stemvitae Multivitamin 30oz in an FDA Class I enforcement action reported as F-1431-2016. Undeclared whey protein which contains the allergens of milk and soy lecithin.

What are the symptoms of Undeclared milk exposure?

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a milk allergy.

How quickly can Undeclared milk symptoms appear?

Reactions can begin within minutes to a few hours after eating the product.

Who is most at risk from Undeclared milk?

People with a diagnosed cow's milk allergy, especially children and anyone with a history of anaphylaxis.

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have a milk allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

How do I get a refund from Nuvi Global Corporation?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-1431-2016 and keep the packaging, lot code and proof of purchase if you have them.

Is the Nuvi Global Corporation recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1431-2016. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.