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Stop using now Food recall · FDA · Published February 10, 2020

Blendtopia Superfood Smoothie Kit Glow Flavor Recall: Listeria Contamination Risk

Blendtopia recalls Glow flavor smoothie kits due to potential Listeria monocytogenes contamination. Consumers should check product dates and lot numbers for affected items.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #F-0759-2020FoodBlendtopia ›
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Contact the company

Recalling firmBlendtopia Products, LLC1903 W Main St · Troy, OH 45373-1165
✎ GovInfoNow plain-language explainer

Blendtopia is recalling its Glow flavor Superfood Smoothie Kit in 7 oz flexible pouches because they may contain Listeria monocytogenes. This contamination risk could cause serious illness, so affected consumers should stop using the product. Read more at govinfonow.com/recall/15946-blendtopia-superfood-smoothie-kit-glow-flavor-recall-listeria-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/15946-blendtopia-superfood-smoothie-kit-glow-flavor-recall-listeria-contamination-risk · Updated October 5, 2026 · FDA enforcement record: FDA #F-0759-2020

Cite this page

“Blendtopia Superfood Smoothie Kit Glow Flavor Recall: Listeria Contamination Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/15946-blendtopia-superfood-smoothie-kit-glow-flavor-recall-listeria-contamination-risk. Based on FDA recall #F-0759-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0759-2020%22&limit=1).

The FDA announced on Feb. 10, 2020, that Blendtopia Products, LLC voluntarily recalled its Superfood Smoothie Kit Glow flavor due to potential Listeria monocytogenes contamination. The agency said consumers should not consume the product.

How to tell if you have it

  • Brand: Blendtopia
  • Product: Blendtopia Superfood Smoothie Kit Glow flavor, 7 oz flexible pouch
  • UPC: 868372000208
  • Best By dates: July 2021, Oct 2021, Nov 2021
  • Lot codes: 19204, 19276, 19289, 19309

The hazard

The product poses a potential contamination of Listeria monocytogenes. The FDA classified the recall as Class I.

Context

GovInfoNow's records show other recent recalls involving Listeria risks include La Colonia Foods Requeson Bulk Product Recall (2026-06-04), CUISINE KETTLE Tomato Bisque Soup Kit Recall (2026-08-11), and Moonlight Packing Peppermint Peaches Recall (2025-10-28).

How to tell if you have this one

Check for the Glow flavor label on the 7 oz flexible pouch. Look for Best By dates from July to November 2021 and lot numbers 19204, 19276, 19289, or 19309. The UPC code is 868372000208.

  • Brand
    Blendtopia
  • Product
    Blendtopia Superfood Smoothie Kit Glow flavor, 7 oz flexible pouch
  • Category
    Food
FDA recall event · 5 products

All 5 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Terminated
  • Distribution
    CA, CO, CT, FL, GA, IA, IN, NH, NV, NY, OH, PA, SC, TN, TX, VT, WA, WI
Recall numberProduct, codes & lotsQuantity
F-0759-2020Blendtopia Superfood Smoothie Kit Glow flavor, 7 oz flexible pouch; Best By July 2021, Best By Oct 2021, Best By Nov 2021; including lots 19204, 19276, 19289, 19309; UPC Code: 8683720002089,795 cases.
F-0760-2020Blendtopia Superfood Smoothie Kit Detox flavor, 7 oz flexible pouch; Best By July 2021, Best By Oct 2021, Best By Nov 2021; including lots 19204, 19276, 19289, 19309; UPC Code: 8683720002159,963 cases.
F-0761-2020Blendtopia Superfood Smoothie Kit Immunity flavor, 7 oz flexible pouch; Best By July 2021, Best By Oct 2021, Best By Nov 2021; including lots 19204, 19276, 19289, 19309; UPC Code: 8683720002224,684 cases
F-0762-2020Blendtopia Superfood Smoothie Kit Strength flavor, 7 oz flexible pouch; Best By July 2021, Best By Oct 2021, Best By Nov 2021; including lots 19204, 19276, 19289, 19309; UPC Code: 8683720002393,347 cases.
F-0763-2020Blendtopia Superfood Smoothie Kit Energy flavor, 7 oz flexible pouch; Best By July 2021, Best By Oct 2021, Best By Nov 2021; including lots 19204, 19276, 19289, 19309; UPC Code: 86837200024610,931 cases.
Based on the official FDA remedy

What to do — step by step

  1. Stop Using It Now

    Immediately discard any Glow flavor Superfood Smoothie Kit pouches with Best By dates from July to November 2021 and lot numbers 19204, 19276, 19289, or 19309.

Where it went and when

Where it was distributed

Distributed in 18 states.

Alaska: not listedAKMaine: not listedMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: yesWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: yesNVWyoming: not listedWYSouth Dakota: not listedSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: not listedNJConnecticut: yesCTCalifornia: yesCAUtah: not listedUTColorado: yesCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: yesTNNorth Carolina: not listedNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: yesFL

FDA distribution: “CA, CO, CT, FL, GA, IA, IN, NH, NV, NY, OH, PA, SC, TN, TX, VT, WA, WI” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Colorado, Connecticut, Florida, Georgia, Indiana, Iowa, Nevada, New Hampshire, New York, Ohio, Pennsylvania, South Carolina, Tennessee, Texas, Vermont, Washington, Wisconsin.

Recall timeline

FDA terminated this recall 2.1 years after the firm started it.

1. Firm started the recall: Feb 10, 202012. FDA classified it Class I: Feb 28, 202023. Published in FDA’s Enforcement Report: Mar 11, 202034. FDA terminated the recall: Feb 28, 2022420202022
  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.

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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-0759-2020 (February 10, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0759-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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