Professional Botanicals MealP: Undeclared Milk Allergen in Dietary Supplements
Professional Botanicals recalls MealPlex and Veo Natural Pearl 3.0 dietary supplements due to undeclared milk allergen. Consumers should check product labels and contact the company for details.
Lower-risk recall
Professional Botanicals announces a voluntary field action for MealPlex and Pearl due to undeclared milk allergen.
Contact the company
What happened, in plain English
Professional Botanicals is recalling two dietary supplements, MealPlex and Veo Natural Pearl 3.0, because they contain undeclared milk allergen. This poses a risk for people with milk allergies who may experience allergic reactions. Read more at govinfonow.com/recall/23064-professional-botanicals-mealp-undeclared-milk-allergen-in-dietary-supplements.
Source Summary by GovInfoNow · govinfonow.com/recall/23064-professional-botanicals-mealp-undeclared-milk-allergen-in-dietary-supplements · Updated October 9, 2026 · FDA enforcement record: FDA #F-0351-2017
Cite this page
“Professional Botanicals MealP: Undeclared Milk Allergen in Dietary Supplements.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23064-professional-botanicals-mealp-undeclared-milk-allergen-in-dietary-supplements. Based on FDA recall #F-0351-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0351-2017%22&limit=1).
Why it’s dangerous
The supplements contain milk allergen without being declared on the label. This can cause allergic reactions in individuals with milk allergies, including symptoms like hives, swelling, or difficulty breathing.
Who’s affected
People who have milk allergies or are sensitive to dairy products are at risk. Those who have consumed the recalled supplements may need to seek medical advice.
How to tell if you have this one
Check for the product names 'MealPlex (756 grams)' or 'Veo Natural Pearl 3.0 (378 grams)' in plastic tub containers. The lot number is 032119.
- Brand
Professional Botanicals- Category
Food
What to do — step by step
Check Product Label
Look for the product names and lot number on the container.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Nationwide. No VA/govt/military, Canadian, or other foreign consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 8 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0351-2017 (October 5, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0351-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.