Imu-Tek recalls 7oz Immuno-5 Colostrum Powder due to undeclared milk allergen. This dietary supplement may cause allergic reactions in people with milk allergies. Consumers should check packaging for lot number 216.
Undeclared milk allergen
Imu-Tek is recalling its Immuno-5 Colostrum Powder (7 oz) because it contains an undeclared milk allergen. This poses a risk for people with milk allergies who might experience allergic reactions. The product is intended as a dietary supplement for humans but some customers use it for pets.
The product contains an undeclared milk allergen that could trigger allergic reactions in people with milk allergies. This is a risk because the product is marketed as a dietary supplement but some users may consume it without knowing the allergen is present.
People who consume this dietary supplement for humans or pets may be affected. Those with milk allergies are at higher risk of allergic reactions.
Check for the product name 'Immuno-5 Colostrum Powder' (7 oz) with UPC 738654000335. Look for lot number 216 on the packaging. The expiration date is April 16, 2027.
Look for the lot number 216 and expiration date of April 16, 2027 on the plastic jar with sealed lid.
No, this product contains an undeclared milk allergen that could cause allergic reactions in people with milk allergies.
The recall does not specify a remedy, so check the product packaging for lot number 216 and expiration date. Contact Imu-Tek at 3541 East Vine Drive, Fort Collins, CO 80524 for further assistance.
The product is intended for humans but some customers use it for pets. However, the recall is for human consumption due to the undeclared milk allergen.
We’ve drafted a message you can send Imu-Tek to request your refund or repair — edit it as you like.
Subject: Recall H-0483-2026 — Imu-Tek Imu-Tek Hello, I own a Imu-Tek that is covered by recall H-0483-2026 from Imu-Tek. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
