CLASS I Food recall · Reported 13 Apr 2016 · FDA Enforcement Report

VPro Raw Plant Protein, Natural recalled by NutraKey

NutraKey is recalling VPro Raw Plant Protein, Natural, distributed nationwide in the US. The recall was initiated on 15 Jan 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUPC 820103456432, LOT VP004617 (EXP 07/2017) and LOT VP004688 (EXP 02/2018).
Quantity recalledTotal product including all flavors: 17,730 total units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1038-2016
FDA event ID
73277
Recalling firm
NutraKey, Longwood, FL
Brand
VPro
Classification
Class I
Status
Terminated
Recall initiated
15 Jan 2016
FDA classified
6 Apr 2016
Reported
13 Apr 2016
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Soy
Product category
Other

Timeline

15 Jan 2016Recall initiated by company
6 Apr 2016Classified by FDA+82 days
13 Apr 2016Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared Soy

Product as listed by the FDA

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

Where it was distributed

Nationwide.

Nationwide

Questions about this recall

Is VPro Raw Plant Protein, Natural recalled?

Yes. NutraKey recalled VPro Raw Plant Protein, Natural on 15 Jan 2016. The recall is Class I and its status is Terminated. Recall number F-1038-2016.

Why was it recalled?

Undeclared Soy

Which lots are affected?

UPC 820103456432, LOT VP004617 (EXP 07/2017) and LOT VP004688 (EXP 02/2018).

Where was it sold?

Nationwide.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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