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FDA recall, , Moderate risk

Imu-Tek Immuno-5 Colostrum Powder

Imu-Tek Immuno-5 Colostrum Powder contains an undeclared milk allergen.

Recall ended Aug 14, 2026. Still check yours.

What happened

Imu-Tek Animal Health, Incorporated, of Fort Collins, Colorado, recalled Imu-Tek Immuno-5 Colostrum Powder 7 oz., a dietary supplement for people, because it contains an undeclared milk allergen. The recall began November 25, 2025, and was added to the FDA's Enforcement Report on February 5, 2026. The product was sold in Arizona, California, Colorado, Florida, Massachusetts, Maine, Minnesota, North Carolina, New Hampshire, Oklahoma, Rhode Island, Tennessee, Texas, Utah and Wisconsin.

What to do

We don't have product-specific instructions for this recall. FDA's general advice for food recalls:

  1. Return it to the store where you bought it, or throw it away.
  2. Don't give it to anyone else, such as a food bank, or to a pet.

Is yours affected?

Match the list below, then check the codes the FDA notice also names.

A UPC is the number printed under a barcode.

  1. Imu-Tek Immuno-5 Colostrum Powder

    UPC
    • 7 38654 00033 5
    Lot code
    • 216

From the FDA notice

UPC:7 38654 00033 5 Firm name on label: Imu-Tek, 3541 East Vine Drive, Fort Collins, CO 80524

Recall details

Company began the recall
Company
Imu-Tek Animal Health, IncorporatedFort Collins, Colorado
Risk

Moderate risk

Eating it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.

FDA Class II recall · How risk is rated

Event ID
98082
Recall number
H-0483-2026
Quantity recalled
113 bottles

All recalls from Imu-Tek Animal Health, Incorporated

Timeline

FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.

  1. Company began the recall

  2. Added to FDA's Enforcement Report · Classified by FDA

  3. In FDA's weekly enforcement report

  4. Recall ended

  5. Listed on Recall Canary

Summary by Recall Canary, written with AI · summary updated Oct 23, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)