StemVida International recalls StemAlive 90 Capsules due to undeclared milk content. Affected lots have specific expiration dates and are sold through independent distributors.
Stemvida International Corporation of Ontario California is recalling certain lots of StemAlive 90 Capsules, because it contains undeclared milk.
StemVida International is recalling certain lots of StemAlive 90 Capsules because they contain undeclared milk. This poses a risk for people with milk allergies who may experience allergic reactions. Consumers should check the lot numbers and expiration dates listed in the recall notice.
The capsules contain undeclared milk, which can trigger allergic reactions in individuals with milk allergies. This is a food safety issue that affects consumers who are sensitive to dairy products.
People with milk allergies are at risk of allergic reactions from consuming these capsules. The product is sold through independent distributors and is available in specific lot numbers with expiration dates.
Check for the white plastic bottle with white lid and the white and gold label. The product has specific lot numbers and expiration dates listed in the recall notice.
Identify the lot number and expiration date on the bottle to determine if it's affected.
The product contains undeclared milk, which can cause allergic reactions in people with milk allergies.
Check the lot number and expiration date to see if it's affected. If it is, stop using it and contact StemVida International for further instructions.
Look for the white plastic bottle with white lid and white and gold label. Check the lot numbers and expiration dates listed in the recall notice.
We’ve drafted a message you can send StemVida to request your refund or repair — edit it as you like.
Subject: Recall F-1536-2014 — StemVida StemVida Hello, I own a StemVida that is covered by recall F-1536-2014 from StemVida. 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.
