RECALL RECORD — CLASS IIRecall closedF-0860-2022/FDA enforcement

Herbalife Nutritionprotein Bar Deluxe - Chocolate Peanut Flavor

What you need to know

Class II
  • What happened

    Undeclared allergen - egg

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. 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 FDANationwide (US)More food

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Product identification

Source: FDA FOOD

Brand nameHerbalife International of America
Recalling firmHerbalife International of AmericaLos Angeles, CA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot code G221684A EXP Date 10/2022
Distribution area
Nationwide

Nationwide distribution

United States

Quantity affected13, 820 + 23 bars distributed as kits
Recall initiationFDA report date: March 23, 2022
FDA recall numberF-0860-2022

Beyond the headline

The recall, in context

Herbalife International of America initiated this food recall on March 1, 2022. The FDA enforcement report states: Undeclared allergen - egg. The FDA report lists distribution as: Nationwide distribution.

The FDA enforcement report describes the reason as: Undeclared allergen - egg

Herbalife Nutritionprotein Bar Deluxe - Chocolate Peanut Flavor was made or distributed by Herbalife International of America in Los Angeles, CA, United States. This page reflects FDA report F-0860-2022, dated March 23, 2022.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. 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 may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

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 egg

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with an egg 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 egg allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have an egg 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 Herbalife Nutritionprotein Bar Deluxe - Chocolate Peanut Flavor recall?

Herbalife International of America recalled Herbalife Nutritionprotein Bar Deluxe - Chocolate Peanut Flavor in an FDA Class II enforcement action reported as F-0860-2022. Undeclared allergen - egg

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 an egg 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.

Is the Herbalife International of America 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-0860-2022. 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

Brand history

More recalls by Herbalife International of America

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