CLASS I Food recall · Reported 10 Dec 2025 · FDA Enforcement Report

Genepro Whey 4th Generation Plasma Treated Protein, unflavored recalled

Genepro Protein is recalling Genepro Whey 4th Generation Plasma Treated Protein, unflavored, distributed in 37 states. The recall was initiated on 12 Nov 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot: 250214 Best By Date: 2-13-2027
Quantity recalled250 bags

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
H-0302-2026
FDA event ID
98013
Recalling firm
Genepro Protein, Cary, NC
Classification
Class I
Status
Terminated
Recall initiated
12 Nov 2025
FDA classified
11 Dec 2025
Reported
10 Dec 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Milk
Product category
Protein Powder

Timeline

12 Nov 2025Recall initiated by company
10 Dec 2025Published in enforcement report+28 days
11 Dec 2025Classified by FDA+1 day

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

Reason for recall

Product is mislabeled - the labeling contains incorrect ingredient information and fails to declare milk as an allergen

Product as listed by the FDA

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

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

AlabamaArkansasArizonaCaliforniaColoradoConnecticutFloridaGeorgiaIowaIllinoisIndianaMassachusettsMarylandMinnesotaMissouriMississippiNorth CarolinaNorth DakotaNew HampshireNew Jersey

Questions about this recall

Why was it recalled?

Product is mislabeled - the labeling contains incorrect ingredient information and fails to declare milk as an allergen

Which lots are affected?

Lot: 250214 Best By Date: 2-13-2027

Where was it sold?

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

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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