FDA Announces Recall of Imu-Tek Colostrum-5 Powder
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
The FDA has initiated a recall of 64 bottles of Imu-Tek Colostrum-5 Powder due to potential under-processing, affecting multiple U.S. states.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 14, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Food.
What Happened
The FDA has announced a recall for Imu-Tek Colostrum-5 Powder because the product is potentially under-processed.
Which Products Are Affected
The affected product is Imu-Tek Colostrum-5 Powder; 30% IgG, 1,000 mg 2x/day, orally with 8 ounces of water, to support a healthy immune system, with a 3-year shelf life, in a 24-ounce (680 grams) plastic bottle featuring an inner liner seal and shrink band exterior seal. It has UPC 7 38654 00052 6, Lot #22, and expiration 020528. A total of 64 bottles were 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, and WY. The official recall number is H-0661-2026.
What You Should Do
Consumers who have the affected product should contact Imu-Tek Animal Health, Incorporated at 3541 E Vine Dr, Fort Collins, CO 80524-9238 for instructions on returns or refunds. The recall was initiated through methods such as email, fax, letter, press release, telephone, or visit.
Why This Matters
This recall highlights potential safety issues with under-processed food products, which could lead to health concerns. As a Class II recall, the risks are not immediately life-threatening but may cause temporary or reversible adverse effects.
Source
Information from the FDA, Recall Number H-0661-2026.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,356 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to April 14, 2026.
Frequently Asked Questions
Common questions about this FDA recall.