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Lower risk Food recall · FDA · Published February 4, 2021

Tropicana KeVita Cucumber Rosemary Recall: Mislabeling in Refrigerated Cases

Tropicana recalls KeVita Cucumber Rosemary 15.2 oz. glass bottles due to mislabeling in refrigerated cases. Consumers should check case codes and use by dates to identify affected products.

🇺🇸 FDA recall #F-0434-2021FoodTropicana ›
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Recalling firmTropicana Products, Inc.1001 13th Ave E · Bradenton, FL 34208-2656
✎ GovInfoNow plain-language explainer

What happened, in plain English

Tropicana is recalling KeVita Cucumber Rosemary drinks because they were mislabeled inside refrigerated cases. This mislabeling means consumers might receive the wrong product, but it doesn't pose a safety risk. Read more at govinfonow.com/recall/14863-tropicana-kevita-cucumber-rosemary-recall-mislabeling-in-refrigerated-cases.

Source Summary by GovInfoNow · govinfonow.com/recall/14863-tropicana-kevita-cucumber-rosemary-recall-mislabeling-in-refrigerated-cases · Updated October 4, 2026 · FDA enforcement record: FDA #F-0434-2021

Cite this page

“Tropicana KeVita Cucumber Rosemary Recall: Mislabeling in Refrigerated Cases.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14863-tropicana-kevita-cucumber-rosemary-recall-mislabeling-in-refrigerated-cases. Based on FDA recall #F-0434-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0434-2021%22&limit=1).

Why it’s dangerous

The mislabeling means that the product inside the case might not match what's listed on the label. This could lead to confusion about which product was actually purchased, but it doesn't cause physical harm or safety issues.

Who’s affected

Anyone who purchased KeVita Cucumber Rosemary 15.2 oz. glass bottles in refrigerated cases with case code 060621PYAA11 or use by date June 6, 2021. People who bought these products from stores that sold them in cases with the specific codes are most at risk.

How to tell if you have this one

Check for case code 060621PYAA11 and use by date June 6, 2021 on the product packaging. The product is a 15.2 oz. glass bottle in a case of six packages, sold in refrigerated storage.

  • Brand
    Tropicana
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for case code 060621PYAA11 and use by date June 6, 2021 on the product packaging.

Where it went and when

Where it was distributed

Distributed in 12 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: yesNDMinnesota: not listedMNIllinois: not listedILWisconsin: yesWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: yesLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: yesFL

FDA distribution: “The product was disturbed to the various states : FL, TX, IA, OH, LA, GA, IN, MO, WI, ND, IN, NC,PA, TX,” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida, Georgia, Indiana, Iowa, Louisiana, Missouri, North Carolina, North Dakota, Ohio, Pennsylvania, Texas, Wisconsin.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Feb 4, 202112. FDA classified it Class II: Apr 16, 202123. Published in FDA’s Enforcement Report: Apr 28, 202134. FDA terminated the recall: May 19, 202142021
  1. Firm started the recall
  2. FDA classified it Class II
  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-0434-2021 (February 4, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0434-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 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