Genepro Whey 4th Generation Plasma Treated Protein recall
Recalled by Genepro Protein, Inc.
The product, as the FDA describes it: Genepro Whey 4th Generation Plasma Treated Protein, unflavored, Net Wt. 225g, 30 servings, packaged in a resealable mylar bag, UPC 850053365126, Manufactured For: Genepro Protein, Inc. 15000 Weston Parkway, Cary NC 27513 Front label reads, in part: "* LACTOSE FREE * DAIRY FREE *ALLERGEN FREE" Back label reads, in part: "OTHER INGREDIENTS: Hydrolyzed NiHPRO ProteinIsolate (Pea Protein Isolate, Rice Protein Isolate, Mungbean Protein Isolate, L-Lysine, L-Leucine, L-Threonine, L-Methionine). CONTAINS: Pea, Rice
Why it was recalled
Product is mislabeled - the labeling contains incorrect ingredient information and fails to declare milk as an allergen
The FDA has since closed this recall out, which means the company finished removing the product from sale. It is kept here because a closed recall still matters to anyone holding a package bought before it ended.
What to do if you have it
This is a labelling failure rather than spoiled food, so it matters entirely to whoever eats it. If nobody in your household reacts to what went undeclared here, the product is not dangerous to you, though you can still return it. If somebody does, treat every package from the affected run as unsafe no matter how much has already been eaten without incident.
How to tell whether your package is one of them
A recall covers particular production runs, not everything the company makes, so the codes decide it. These are the ones the FDA published. Match them against what is printed on your package, usually near the best-before date.
Lot: 250214 Best By Date: 2-13-2027
The details on record
| Recalling company | Genepro Protein, Inc. |
|---|---|
| Company location | Cary, NC |
| Where it was distributed | AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, MA, MD, MN, MO, MS, NC, ND, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WY |
| How much was recalled | 250 bags |
| Recall started | November 12, 2025 |
| Published by the FDA | December 10, 2025 |
| Recall type | Voluntary: Firm initiated |
| How the company announced it | |
| FDA recall number | H-0302-2026 |
Everything above comes from the FDA enforcement report for this recall. Read the official notice for the company's own wording, contact numbers, and any photographs of the packaging.
The other half of the answer
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