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Use caution Food recall · FDA · Published October 7, 2026

Pur Aqua Sparkling Frost Cherry Limeade Recall: Undeclared Aspartame

Refresco Beverages recalls Pur Aqua Sparkling Frost Cherry Limeade 17 oz. due to undeclared aspartame, which may cause allergic reactions.

🇺🇸 FDA recall #H-0095-2027FoodPur Aqua ›
✎ GovInfoNow plain-language explainer

Refresco Beverages US Inc is recalling Pur Aqua Sparkling Frost Cherry Limeade 17 oz. bottles because they may contain undeclared aspartame. This matters because people with phenylketonuria (PKU) or those avoiding aspartame for other reasons could be exposed to an ingredient not listed on the label. The recall involves approximately 2,100 units distributed in Florida and downstream retail stores. Read more at govinfonow.com/recall/1749429-refresco-beverages-us-inc-recalls-pur-aqua-sparkling-frost-cherry.

Source Summary by GovInfoNow · govinfonow.com/recall/1749429-refresco-beverages-us-inc-recalls-pur-aqua-sparkling-frost-cherry · Published October 27, 2026 · Updated October 27, 2026 · Official notice: FDA #H-0095-2027

Cite this page

“Pur Aqua Sparkling Frost Cherry Limeade Recall: Undeclared Aspartame.” GovInfoNow, updated October 27, 2026. https://govinfonow.com/recall/1749429-refresco-beverages-us-inc-recalls-pur-aqua-sparkling-frost-cherry. Based on FDA recall #H-0095-2027.

Refresco Beverages US Inc voluntarily recalled Pur Aqua Sparkling Frost Cherry Limeade 17 oz. due to undeclared aspartame, the FDA said on Oct. 7, 2026.

How to tell if you have it

  • Brand: Pur Aqua
  • Product: Sparkling Frost Cherry Limeade
  • Size: 17 oz.
  • UPC: 4099100167023
  • Best if use by: 032327 TA

The hazard

The product may contain undeclared aspartame.

Context

GovInfoNow's records show Refresco Beverages US Inc has issued three other recalls since July 7, 2022. Other recent recalls of similar products include Domino Foods Sodexo Stars Saccharin Pink Packets Recall (Jan. 13, 2026) and Loard's Coconut Pineapple Ice Recall (April 15, 2026).

How to tell if you have this one

Check if you have Pur Aqua Sparkling Frost Cherry Limeade in a 17 oz. bottle. Verify the UPC is 4099100167023 and the 'Best if use by' date is 032327 TA. These products were sold in Florida and potentially at other retail stores.

  • Brand
    Pur Aqua
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check your product

    Verify the UPC 4099100167023 and best if use by date 032327 TA on the bottle.

  2. Avoid consumption

    Do not consume the product if you have PKU or are avoiding aspartame, as it may contain undeclared ingredients.

Where it went and when

Where it was distributed

Distributed in Florida.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “Florida with further downstream distribution to retail stores” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida.

Recall timeline

FDA published this recall 14 days after the firm started it.

1. Firm started the recall: Oct 7, 202612. FDA classified it Class III: Oct 15, 202623. Published in FDA’s Enforcement Report: Oct 21, 202634. Added to GovInfoNow: Oct 27, 202642026
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. Added to GovInfoNow

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 #H-0095-2027 (October 7, 2026)
  • Plain-language summary written by qwen3.6:35b-a3b on October 27, 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