Food Recall Check
Class I · High risk Terminated Initiated Sep 18, 2018 (8 years ago)

Purus Labs MYOWHEY Premium Whey Protein recall

Recalled by Purus Labs, Inc. · Plano, TX, United States

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

Why it was recalled

Undeclared milk and soy.

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

Purus Labs MYOWHEY Premium Whey Protein, Chocolate Cookie Crunch, 75 True Servings, Net Wt. 5 lb / 2.26 kg. UPC 55734-00285. Manufactured for and distributed by Purus Labs, 2601 Resource Drive, Plano, TX 75704

Quantity: 1280 (156 US, 1124 OUS)

Food: Chocolate & candy Bread & bakery

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.

PL:0100518

Where it was sold

Arkansas Connecticut Florida Michigan North Carolina Nevada Oklahoma Texas Virginia

FDA's distribution note: Within the US: AR, CT, FL, MI, NC, NV, OK, TX, VA. Outside the US: Chile and United Arab Emirates

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
Purus Labs, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 18, 2018
In FDA report of
Oct 10, 2018
Terminated
Feb 5, 2019
FDA recall number
F-0005-2019 · event 81056
Official record
FDA enforcement report search

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