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ACTIVE RECALL — CLASS IIActive recallF-0261-2025/FDA enforcement
Nestle Health Science·Food·Nov 5, 2024

Nestle Health Services Nutren 2.0 Kcal/ml, Calorically Dense Complete Nutrition with Fiber…

What you need to know

Class II

  • What happened

    Labeling Error. Nutren 2.0 UltraPak pouches were mislabeled with an Isosource 1.5 label.

  • 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.

Active recall · classified by the FDAAZ, CA, FL, GA +12 moreMore food

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Product identification

Source: FDA FOOD

Brand nameNestle Health Science
Recalling firmNestle Health ScienceBridgewater, NJ, United States
UPC / barcodes
0 43900 18181 3
Lot / date codes
  • Lot number: 4213572151 Expiration Date: 7/31/2025
Distribution area
AZCAFLGAILINLAMAMDMOMSNYOHPATXVA

AZ, CA, FL, GA, IL, IN, LA, MA, MD, MO, MS, NY, OH, PA, TX, VA

United States

Quantity affected959 cases (5754 pouches)
Recall initiationFDA report date: December 18, 2024
FDA recall numberF-0261-2025

Beyond the headline

The recall, in context

Nestle Health Science initiated this food recall on November 5, 2024. The FDA enforcement report states: Labeling Error. Nutren 2.0 UltraPak pouches were mislabeled with an Isosource 1.5 label. The FDA report lists distribution as: AZ, CA, FL, GA, IL, IN, LA, MA, MD, MO, MS, NY, OH, PA, TX, VA.

The FDA enforcement report describes the reason as: Labeling Error. Nutren 2.0 UltraPak pouches were mislabeled with an Isosource 1.5 label.

Nestle Health Services Nutren 2.0 Kcal/ml, Calorically Dense Complete Nutrition with Fiber… was made or distributed by Nestle Health Science in Bridgewater, NJ, United States. This page reflects FDA report F-0261-2025, dated December 18, 2024.

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 UPC and lot code 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 allergen

Symptoms to watch for

Hives, swelling, wheezing, coughing, vomiting, abdominal pain or a drop in blood pressure. Anaphylaxis is a medical emergency.

When symptoms may appear

Allergic reactions often begin within minutes to a few hours of eating the allergen.

Higher-risk groups

Anyone with a diagnosed food allergy, especially children, and people with a history of anaphylaxis or asthma.

What to do now

  1. 1Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy.
  2. 2If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services.
  3. 3Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

For a severe allergic reaction, do not wait for a callback or refund process before seeking emergency care.

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 Nestle Health Services Nutren 2.0 Kcal/ml, Calorically Dense Complete Nutrition with Fiber… recall?

Nestle Health Science recalled Nestle Health Services Nutren 2.0 Kcal/ml, Calorically Dense Complete Nutrition with Fiber… in an FDA Class II enforcement action reported as F-0261-2025. Labeling Error. Nutren 2.0 UltraPak pouches were mislabeled with an Isosource 1.5 label.

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 or serve the affected product if you or anyone in the household has a diagnosed allergy. If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services. Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

Is the Nestle Health Science recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0261-2025. 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.