Imu-Tek Immuno-5 Colostrum Powder 7 oz. Intended Use: Dietary Supplement for People. (Some customers use this for th
Summary
The FDA issued a Class II for Imu-Tek Immuno-5 Colostrum Powder 7 oz. Intended Use: Dietary Supplement for by Imu-Tek Animal Health, Incorporated. Reason: Undeclared milk allergen.
Details
Source
Food Recall
External ID
H-0483-2026
Action Date
2026-02-11
Status
Ongoing
Category
food
Product Description
Imu-Tek Immuno-5 Colostrum Powder 7 oz. Intended Use: Dietary Supplement for People. (Some customers use this for their pets).Packaging: Plastic jar with Sealed lid. Net Weight: 7 ounces. UPC:7 38654 00033 5 Firm name on label: Imu-Tek, 3541 East Vine Drive, Fort Collins, CO 80524
Lot/Code Info: Lot #216, Expiration 4/16/2027
Quantity Affected: 113 bottles
Reason for Recall
Undeclared milk allergen
Distribution
Distributed in : AZ, CA, CO, FL, MA, ME, MN, NC, NH, OK, RI, TN, TX, UT, and WI.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-11-25
Company
Fort Collins, CO
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 69 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Imu-Tek Animal Health, Incorporated has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Imu-Tek Animal Health, Incorporated) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Imu-Tek Animal Health, Incorporated have FDA actions?
Imu-Tek Animal Health, Incorporated has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0483-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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