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Stop using now Food recall · FDA · Published March 2, 2020

ReStructure Vanilla Protein Powder Recall: Undeclared Milk Allergen

New Capstone, Inc. recalls ReStructure Vanilla Protein Powder because the label fails to declare milk, posing a risk to those with allergies.

🇺🇸 FDA recall #F-0871-2020FoodReStructure ›
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Recalling firmNew Capstone, Inc255 Marietta Rd · Mooresville, NC 28117-8426
✎ GovInfoNow plain-language explainer

New Capstone, Inc. is recalling ReStructure Vanilla Protein Powder because the ingredient list does not include the word "milk," even though it contains whey protein concentrate derived from milk. This omission poses a serious health risk to individuals with milk allergies or severe dairy sensitivities who may unknowingly consume the product. The recall covers specific lots distributed nationwide. Read more at govinfonow.com/recall/15821-restructure-vanilla-protein-powder-recall-undeclared-milk-allergen.

Source Summary by GovInfoNow · govinfonow.com/recall/15821-restructure-vanilla-protein-powder-recall-undeclared-milk-allergen · Updated October 11, 2026 · FDA enforcement record: FDA #F-0871-2020

Cite this page

“ReStructure Vanilla Protein Powder Recall: Undeclared Milk Allergen.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/15821-restructure-vanilla-protein-powder-recall-undeclared-milk-allergen. Based on FDA recall #F-0871-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0871-2020%22&limit=1).

The FDA announced on March 2, 2020, that New Capstone, Inc. is recalling ReStructure Vanilla Protein Powder due to undeclared milk allergens. The firm initiated this voluntary Class I recall after discovering the labeling omitted milk from the ingredient statement.

How to tell if you have it

  • Brand: ReStructure
  • Product: VANILLA PROTEIN POWDER NET WT. 527G POUCH & 27G SINGLE PACKET Other Ingredients: Non-GMO rBGH-Free Whey
  • UPC: 00867780000206
  • Lot#: 19211
  • Expiration Date: 06/21

The hazard

The product labeling does not include the word milk on the ingredient statement, posing an allergen risk to consumers with milk sensitivities. The FDA classified this as a Class I recall, indicating a high probability of serious adverse health consequences.

Context

GovInfoNow's records show other recent recalls involving undeclared milk include The Better Bakehouse Donutful Donuts (2026-08-17) and Loard's Vanilla Ice Cream (2026-04-15). Additional similar recalls of products with undeclared milk allergens include Imu-Tek Immuno-5 Colostrum Powder (2025-11-25).

How to tell if you have this one

Check for ReStructure Vanilla Protein Powder in either a 527g pouch or a 27g single packet. Look for UPC 8 67780 00020 6 and Lot #19211 with an expiration date of 06/21. The product was distributed nationwide.

  • Brand
    ReStructure
  • Product
    ReStructure VANILLA PROTEIN POWDER NET WT. 527G POUCH & 27G SINGLE PACKET Other Ingredients: Non-GMO rBGH-Free Whey
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat or drink the recalled ReStructure Vanilla Protein Powder due to the undeclared milk allergen.

  2. Check your lot number

    Verify if your product matches Lot #19211 and UPC 8 67780 00020 6.

  3. Contact the manufacturer

    Call New Capstone, Inc. at 1-888-577-3703 for further information or instructions.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Product was distributed Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 2.9 years after the firm started it.

1. Firm started the recall: Mar 2, 202012. FDA classified it Class I: Mar 31, 202023. Published in FDA’s Enforcement Report: Apr 8, 202034. FDA terminated the recall: Jan 10, 2023420202023
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

Where was this product sold?

The product was distributed nationwide across the United States.

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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-0871-2020 (March 2, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0871-2020 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA