RECALL RECORD — CLASS IIRecall closedH-0483-2026/FDA enforcement

Imu-tek Immuno-5 Colostrum Powder 7 OZ

What you need to know

Class II
  • What happened

    Undeclared milk allergen

  • 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

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDAIN, AZ, CA, CO +12 moreMore supplements

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Product identification

Source: FDA FOOD

Brand nameImu-tek Animal Health, Incorporated
Recalling firmImu-tek Animal Health, IncorporatedFort Collins, CO, United States
UPC / barcodes
7 38654 00033 5
Lot / date codes
  • Lot #216, Expiration 4/16/2027
Distribution area
INAZCACOFLMAMEMNNCNHOKRITNTXUTWI

Distributed in : AZ, CA, CO, FL, MA, ME, MN, NC, NH, OK, RI, TN, TX, UT, and WI.

United States

Quantity affected113 bottles
Recall initiationFDA report date: February 11, 2026
FDA recall numberH-0483-2026

Beyond the headline

The recall, in context

Imu-tek Animal Health, Incorporated initiated this supplements recall on November 25, 2025. The FDA enforcement report states: Undeclared milk allergen. The FDA report lists distribution as: Distributed in : AZ, CA, CO, FL, MA, ME, MN, NC, NH, OK, RI, TN, TX, UT, and WI.

The FDA enforcement report describes the reason as: Undeclared milk allergen

Imu-tek Immuno-5 Colostrum Powder 7 OZ was made or distributed by Imu-tek Animal Health, Incorporated in Fort Collins, CO, United States. This page reflects FDA report H-0483-2026, dated February 11, 2026.

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 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 Imu-tek Immuno-5 Colostrum Powder 7 OZ recall?

Imu-tek Animal Health, Incorporated recalled Imu-tek Immuno-5 Colostrum Powder 7 OZ in an FDA Class II enforcement action reported as H-0483-2026. Undeclared milk allergen

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. 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.

Is the Imu-tek Animal Health, Incorporated 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 H-0483-2026. 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

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