CLASS I Food recall · Reported 16 Nov 2016 · FDA Enforcement Report

MealPlex and Veo Natural Pearl 3.0 Ultimate Meal Drinks Containers recalled

Professional Botanicals is recalling MealPlex and Veo Natural Pearl 3.0 Ultimate Meal Drinks Containers, distributed nationwide in the US. The recall was initiated on 5 Oct 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot# 032119
Quantity recalled192

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-0351-2017
FDA event ID
75398
Recalling firm
Professional Botanicals, Ogden, UT
Classification
Class I
Status
Terminated
Recall initiated
5 Oct 2016
FDA classified
8 Nov 2016
Reported
16 Nov 2016
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Milk
Product category
Dietary Supplements

Timeline

5 Oct 2016Recall initiated by company
8 Nov 2016Classified by FDA+34 days
16 Nov 2016Published in enforcement report+8 days

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

Reason for recall

Professional Botanicals announces a voluntary field action for MealPlex and Pearl due to undeclared milk allergen.

Product as listed by the FDA

Professional Botanicals MealPlex (756 grams) and Veo Natural Pearl 3.0 (378 grams) Ultimate Meal Drinks in Plastic Tub Containers. Dietary Supplement.

Where it was distributed

Nationwide. No VA/govt/military, Canadian, or other foreign consignees.

Nationwide Virginia

Questions about this recall

Why was it recalled?

Professional Botanicals announces a voluntary field action for MealPlex and Pearl due to undeclared milk allergen.

Which lots are affected?

Lot# 032119

Where was it sold?

Nationwide. No VA/govt/military, Canadian, or other foreign consignees.

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 26 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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