Food Recall Check
Class I · High risk Terminated Initiated Apr 27, 2016 (10 years ago)

Choice Products Xtreme Fiber Detox Net recall

Recalled by World's Choice Products · San Diego, CA, United States

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

Why it was recalled

Undeclared whey protein which contains milk and soy lecithin.

Undeclared allergens: Milk Soy

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

Choice Products. Xtreme Fiber Detox Net. Wt. 1lb Net Wt. 8oz.

Quantity: 2,512 container

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 #15174, 15372, 15423, 15538, 16051

Where it was sold

California Nevada New York Puerto Rico Texas

FDA's distribution note: U.S. distribution to the following; CA, TX, NV, NY, Puerto Rico Foreign distribution to the following; Canada

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, soy; 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
World's Choice Products
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 27, 2016
In FDA report of
Jun 8, 2016
Terminated
Feb 10, 2017
FDA recall number
F-1401-2016 · event 73980
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.