Food recall

Imu-Tek Animal Health, Incorporated recall: Imu-Tek Colostrum-5 120 Capsules

Imu-Tek Animal Health, Incorporated, of Fort Collins, CO, recalled Imu-Tek Colostrum-5 120 Capsules and 1 other product. The FDA's reason: “Product is potentially under-processed.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on February 24, 2026, and the FDA first listed it in its Enforcement Report of April 8, 2026. The company has finished the recall; the FDA hasn't closed it yet.

How serious

Class II

It could cause temporary or minor harm

Why

Other germs or toxins (botulism, hepatitis A, mold...)

Status

Completed

The recall

Company
Imu-Tek Animal Health, Incorporated (Fort Collins, CO)
Reason, in FDA's words
“Product is potentially under-processed.”
Where it was sold
Product distributed in the following states: AK, AL, AZ, CA, CO, CT, FL, HI, IA, ID, IL, IN, MA, MD, MO, MS, NC, NE, NH, NV, NY, OK, OR, SC, TN, TX, UT, WA, WI, WY.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
98486

The 2 products recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-0660-2026 Class II

    Imu-Tek Colostrum-5 120 Capsules; 30% IgG, 2 capsules 2x/day, orally with 8 ounces of water, support a healthy immune system, 3 year shelf life, plastic bottle, inner liner seal and shrink band seal, 500 mg capsule, 7 38654 00026 7, Imu-Tek, Inc. Ft. Collins, CO 80524.

    Codes: Lot #013, 092826 Expiration

    Quantity: 1003 botlles

  • H-0661-2026 Class II

    Imu-Tek Colostrum-5 Powder; 30% IgG,1,000 mg 2x/day, orally with 8 ounces of water, support a healthy immune system, 3 year shelf life, plastic bottle, inner liner seal and shrink band exterior seal, 24 ounces (680 grams) powder, 7 38654 00052 6, ImuTek Laboratories, Fort Collins, CO 80524.

    Codes: Lot #22, 020528 Expiration

    Quantity: 64 bottles

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of April 8, 2026.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.