Food Recall Check
Class I · High risk Terminated Initiated Jan 15, 2016 (11 years ago)

VPro Raw Plant Protein recall

Recalled by NutraKey, Inc. · Longwood, FL, United States

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

Why it was recalled

Undeclared Soy

Undeclared allergen: 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

VPro Raw Plant Protein, Chocolate. Packaged in a plastic bottle with green, white, and black adhesive label. Packaged in 1 lb (15 serving) and 2 lb (30 serving).

Quantity: Total product including all flavors: 17,730 total units

Food: Chocolate & candy

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.

VPro Chocolate 15 serving: UPC 820103309776, LOT VP004341 (EXP 12/2016) and LOT VP125703 (EXP 02/2018). VPro Chocolate 30 serving: UPC 820103309769, LOT VP007668 (EXP 12/2017).

Where it was sold

Nationwide.

FDA's distribution note: Nationwide.

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 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
NutraKey, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 15, 2016
In FDA report of
Apr 13, 2016
Terminated
Aug 23, 2018
FDA recall number
F-1039-2016 · event 73277
Official record
FDA enforcement report search

Also recalled with it (3 more products)

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

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