Severity
Critical
CriticalClass ICompleted
FDA Food recall · Reported December 10, 2025
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). CONT
Product is mislabeled - the labeling contains incorrect ingredient information and fails to declare milk as an allergen
Compiled from official public sources by the editorial team.
Verify with FDA Food →
Genepro Protein, Inc. recalled Genepro Whey 4th Generation Plasma Treated Protein, unflavored, Net Wt. 225g, 30 servings… - a critical-severity action.
Genepro Whey 4th Generation Plasma Treated Protein, unflavored, Net Wt. 225g, 30 servings… was recalled by Genepro Protein, Inc. in December 10, 2025. Reason: Product is mislabeled - the labeling contains incorrect ingredient information and fails to declare milk as a…. Check the official notice for the remedy. Verify recall #H-0302-2026 with the FDA Food before acting.
The recall
Genepro Protein, Inc. issued this critical-severity FDA Food recall-Product is mislabeled - the labeling contains incorrect ingredient information and fails to declare milk as a….
- Critical
- severity level
- Class I
- classification
- December 10, 2025
- reported
Sourced from official FDA Food enforcement records. Verify recall #H-0302-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #H-0302-2026) was formally reported on December 10, 2025, with the manufacturer initiating the action on November 12, 2025. It is classified under Critical severity (Class I), with a current status of Completed. Genepro Protein, Inc. is listed as the recalling firm, operating out of Cary, NC. Federal records list the affected scope as 250 bags.
The documented reason for this recall is: Product is mislabeled - the labeling contains incorrect ingredient information and fails to declare milk as an allergen Distribution data in the federal record shows the product reached: 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. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
250 bags
Related Recalls
6
2 from same agency
Product description
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
Reason for recall
Product is mislabeled - the labeling contains incorrect ingredient information and fails to declare milk as an allergen
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Completed |
| Recall number | H-0302-2026 |
| Date reported | December 10, 2025 |
| Date initiated | November 12, 2025 |
| Recalling firm | Genepro Protein, Inc. |
| Firm location | Cary, NC |
| Affected scope | 250 bags |
| Distribution | 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 |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (H-0302-2026) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Genepro Protein, Inc.. Units affected: 250 bags.
Why was this product recalled? ▼
Product is mislabeled - the labeling contains incorrect ingredient information and fails to declare milk as an allergen
Which agency issued this recall? ▼
This recall was issued by the FDA Food on December 10, 2025. Severity: Critical. Recall number: H-0302-2026.
Where was the recalled product distributed? ▼
Distribution: 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 do I check if my product is affected by a recall? ▼
Check the product description and recall number (H-0302-2026) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported December 10, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.