Food Recall Check
Class I · High risk Terminated Initiated May 20, 2016 (10 years ago)

ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary… recall

Recalled by Ultimate Nutrition, Inc. · Farmington, CT, United States

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

Why it was recalled

Product 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

ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement 1500 mg 325 tablets

Quantity: less than 1000 of all/lots products involved in this recall

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.

Lot/Unit Numbers: 403122, 508080, 604166

Where it was sold

Nationwide.

California Connecticut Idaho North Carolina Pennsylvania

FDA's distribution note: The recalled Amino Gold was distributed nationwide through distributors, stores, and web sites. The product was sold direct to distributors in CA, NC, ID, PA, CT.

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
Ultimate Nutrition, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
May 20, 2016
In FDA report of
Sep 21, 2016
Terminated
Jul 27, 2017
FDA recall number
F-1768-2016 · event 74219
Official record
FDA enforcement report search

Also recalled with it (2 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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