FDA Recall of Imu-Tek Colostrum-5 Capsules Announced
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The FDA has initiated a recall of 1003 bottles of Imu-Tek Colostrum-5 capsules due to potential under-processing, affecting products distributed across 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 read it as a data point about the issuing system: how quickly FDA detected the hazard, how precise the geographic or product-identifier scope is, and whether similar notices have clustered in the same category or region in the last 90 days. Cluster patterns frequently precede a broader regulatory action, a single localized FDA recall is isolated; three of them within a quarter often indicate a supply-chain, infrastructure, or seasonal driver that will keep producing notices until something structural changes.
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What Happened
The FDA has announced a recall for Imu-Tek Colostrum-5 capsules because the product is potentially under-processed, as initiated voluntarily by the recalling firm.
Which Products Are Affected
The affected product is Imu-Tek Colostrum-5 120 Capsules, which contains 30% IgG, with a dosage of 2 capsules twice a day orally with 8 ounces of water to support a healthy immune system. It comes in a plastic bottle with an inner liner seal and shrink band seal, each capsule is 500 mg, and the UPC is 7 38654 00026 7. The recall involves 1003 bottles with Lot #013 and expiration date 092826. These products 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-0660-2026.
What You Should Do
Consumers should contact the recalling firm, Imu-Tek Animal Health, Incorporated, located at 3541 E Vine Dr, Fort Collins, CO 80524-9238, for instructions on returns or refunds. The firm notified consumers via methods including email, fax, letter, press release, telephone, or visit.
Why This Matters
This recall involves a food product that may pose health risks due to potential under-processing, affecting over 1000 bottles distributed nationwide.
Source
Attribution: FDA. For more information, visit the FDA website and search for recall number H-0660-2026.
Original source: FDA Official Notice ↗
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