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Lower risk Food recall · FDA · Published February 24, 2026

Imu-Tek Colostrum-5 Capsules Recall: Under-processed Risk

Imu-Tek recalls Colostrum-: 30% IgG capsules that may be under-processed, posing potential safety risks. Learn if you have affected units and what to do.

🇺🇸 FDA recall #H-0660-2026FoodImu-Tek ›
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Contact the company

Recalling firmImu-Tek Animal Health, Incorporated3541 E Vine Dr · Fort Collins, CO 80524-9238
✎ GovInfoNow plain-language explainer

Imu-Tek is recalling Colostrum-5 capsules that may be under-processed. This could pose a safety risk if the product isn't properly processed. Read more at govinfonow.com/recall/6703-imu-tek-colostrum-5-capsules-recall-under-processed-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/6703-imu-tek-colostrum-5-capsules-recall-under-processed-risk · Updated August 17, 2026 · Official notice: FDA #H-0660-2026

Cite this page

“Imu-Tek Colostrum-5 Capsules Recall: Under-processed Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/6703-imu-tek-colostrum-5-capsules-recall-under-processed-risk. Based on FDA recall #H-0660-2026.

Imu-Tek Animal Health, Incorporated voluntarily recalled Imu-Tek Colostrum-5 120 Capsules due to potential under-processing, according to the FDA on Feb. 24, 2026.

How to tell if you have it

  • Brand: Imu-Tek
  • Product: Imu-Tek Colostrum-5 120 Capsules; 30% IgG
  • UPC: 7 38654 00026 7
  • Lot codes: #013, 092826
  • Expiration date: 092826
  • Quantity: 1003 bottles

The hazard

The product is potentially under-processed.

Context

GovInfoNow's records show Imu-Tek Animal Health, Incorporated has one other recall on record since Nov. 25, 2025: the Imu-Tek Immuno-5 Colostrum Powder Recall for undeclared milk allergen risk. Other recent recalls of similar products include Liquid Blenz Immunity Enhancer Elderberry Recall (April 6, 2026), Blackseed Bitters 16oz/32oz Recall (April 6, 2026), and Menopause Bully 16oz and 32oz Food Recall (April 6, 2026).

How to tell if you have this one

Check for the product name 'Colostrum-5 120 Capsules', 30% IgG, and lot number 013 from the batch dated 092826. The product was sold with a 3-year shelf life.

  • Brand
    Imu-Tek
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Completed
  • Distribution
    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 numberProduct, codes & lotsQuantity
H-0660-2026Imu-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.; Lot #013, 092826 Expiration1003 botlles
H-0661-2026Imu-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.; Lot #22, 020528 Expiration64 bottles
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the product name 'Colostrum-5 120 Capsules', 30% IgG, and lot number 013 from the batch dated 092826.

Where it went and when

Where it was distributed

Distributed in 30 states.

Alaska: yesAKMaine: not listedMEVermont: not listedVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: yesWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: not listedSDIowa: yesIAIndiana: yesINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: yesMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: not listedLAMississippi: yesMSAlabama: yesALGeorgia: not listedGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “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.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Alaska, Arizona, California, Colorado, Connecticut, Florida, Hawaii, Idaho, Illinois, Indiana, Iowa, Maryland, Massachusetts, Mississippi, Missouri, Nebraska, Nevada, New Hampshire, New York, North Carolina, Oklahoma, Oregon, South Carolina, Tennessee, Texas, Utah, Washington, Wisconsin, Wyoming.

Recall timeline

FDA published this recall 43 days after the firm started it.

1. Firm started the recall: Feb 24, 202612. Published in FDA’s Enforcement Report: Apr 8, 202623. FDA classified it Class II: Apr 10, 202632026
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class II

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall states the product may be under-processed, which could pose a safety risk. The official notice does not confirm if it is safe to use.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-0660-2026 (February 24, 2026)
  • Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA