RecallHawk
Class II Recall

Imu-Tek Colostrum-5 Powder; 30% IgG,1,000 mg 2x/day, orally with 8 ounces of water, support a healthy immune system, 3 y

Imu-Tek Animal Health, Incorporated

Summary

The FDA issued a Class II for Imu-Tek Colostrum-5 Powder; 30% IgG,1,000 mg 2x/day, orally with 8 ounces of wat by Imu-Tek Animal Health, Incorporated. Reason: Product is potentially under-processed..

Details

Source

Food Recall

External ID

H-0661-2026

Action Date

2026-04-08

Status

Ongoing

Category

food

Product Description

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.

Lot/Code Info: Lot #22, 020528 Expiration

Quantity Affected: 64 bottles

Reason for Recall

Product is potentially under-processed.

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.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-02-24

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 59 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-0661-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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