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FDA source record Class II Ongoing

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 We...

Recall Date: 2025-11-25 Recalling Firm: Imu-Tek Animal Health, Incorporated Record Ref: H-0483-2026

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns 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 We... and names Imu-Tek Animal Health, Incorporated as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Imu-Tek Animal Health, Incorporated
  • Classification: Class II
  • Status: Ongoing
  • Recall date: 2025-11-25
Best identifiers to check for a FDA record

Compare UPC/GTIN, lot or batch code, package size, flavor or variety, and any best-by/use-by date listed in the notice.

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Product Description & Identification

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

Reason for Recall / Hazard Identified

Undeclared milk allergen

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

Distributed in : AZ, CA, CO, FL, MA, ME, MN, NC, NH, OK, RI, TN, TX, UT, and WI.

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:12 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
H-0483-2026
Indexed update
2026-08-09 21:59:12 UTC
Official source
Open issuing-agency record