Food Recall Check
Class I · High risk Terminated Initiated Jan 17, 2014 (13 years ago)

Stemalive recall

Recalled by Stemvida International INC · Ontario, CA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Stemvida International Corporation of Ontario California is recalling certain lots of StemAlive 90 Capsules, because it contains undeclared milk.

Undeclared allergen: Milk

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

STEMALIVE, 90 Capsules. The product is in a white plastic bottle with white lid, the brand is StemVida International with a white and gold label. Product labeling reads in part:"STEMVIDA INTERNATIONAL***StemAlive***PROMOTES ADULT STEM CELL FUNCTION AND HEALTH***Dietary Supplement***90 Capsules***Formulated exclusively for STEMVIDA International Corporation 4295 Jurupa St Ste 116, Ontario CA 91741***This exclusively formulated product is only available through ETEMVIDA International independent distributors***www.stemvidainternational.com***". The StemAlive product is shipped as a single unit or in boxes of 4 units or 16 units.

Quantity: 458,692

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

The lot numbers and expiration dates are 8419 (Exp.05/2015 and 06/2015), 8486 (Exp.07/2015), 8535 (Exp. 08/2015), 8598 (Exp. 10/2015), 8652 (Exp. 12/2015), 8863 (Exp. 01/2016 and 02/2016), 8872 (Exp. 03/2016), 8873 (Exp. 04/2016 and 05/2016), 9040 (Exp. 08/2016 and 09/2016), 9258 (Exp. 10/2016) and 9314 (Exp. 11/2016).

Where it was sold

Arizona California Colorado Florida New Jersey Nevada New York Oklahoma Texas Utah

FDA's distribution note: " Arizona " California " Colorado " Florida " New Jersey " New York " Nevada " Oklahoma " Texas " Utah

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Stemvida International INC
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 17, 2014
In FDA report of
Feb 26, 2014
Terminated
Mar 31, 2015
FDA recall number
F-1536-2014 · event 67295
Official record
FDA enforcement report search

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