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Lower risk Food recall · FDA · Published February 16, 2018

The Double Cola Company recalls Cherry SKI Lemon Orange Soda: Missing Allergen Labels

The Double Cola Company recalls Cherry SKI Lemon Orange Authentic Citrus Soda 12oz cans due to missing allergen labels for Yellow 5 and Red 40. Consumers should check product codes and contact the company for details.

🇺🇸 FDA recall #F-0908-2018FoodThe Double Cola Company ›
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Contact the company

Recalling firmDouble-Cola Co.-USA dba The Double Cola Company537 Market St Ste 100 · Chattanooga, TN 37402-1229
✎ GovInfoNow plain-language explainer

What happened, in plain English

The Double Cola Company is recalling Cherry SKI Lemon Orange Authentic Citrus Soda 12oz cans because the product label does not list two common allergens: Yellow #5 and Red 40. This recall is important for people with allergies to these dyes to avoid potential reactions. Read more at govinfonow.com/recall/19648-the-double-cola-company-recalls-cherry-ski-lemon-orange-soda.

Source Summary by GovInfoNow · govinfonow.com/recall/19648-the-double-cola-company-recalls-cherry-ski-lemon-orange-soda · Updated October 7, 2026 · FDA enforcement record: FDA #F-0908-2018

Cite this page

“The Double Cola Company recalls Cherry SKI Lemon Orange Soda: Missing Allergen Labels.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19648-the-double-cola-company-recalls-cherry-ski-lemon-orange-soda. Based on FDA recall #F-0908-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0908-2018%22&limit=1).

Why it’s dangerous

The product label does not list Yellow #5 and Red 40, which are common food dyes that some people may be allergic to. Without this information, consumers with these allergies could unknowingly consume the product and experience a reaction.

Who’s affected

People who have purchased the Cherry SKI Lemon Orange Authentic Citrus Soda 12oz cans from the Double Cola Company are affected. Those with allergies to Yellow #5 or Red 40 dyes are at higher risk.

How to tell if you have this one

Check the product code on the can: UPC 071644201030 and lots numbers A8023EV10:25 through A8023EV11:40. The product contains carbonated water, high fructose corn syrup, and lemon juice concentrate.

  • Brand
    The Double Cola Company
  • Product
    Cherry SKI LEMON ORANGE AUTHENTIC CITRUS SODA 12 oz can CONTAINS: CARBONATED WATER, HIGH FRUCTOSE CORN SYRUP, LEMON
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the allergen labels for Yellow #5 and Red 40 on the can. If missing, the product is part of the recall.

Where it went and when

Where it was distributed

Distributed in 4 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: yesINOhio: yesOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: yesKYWest 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: not listedFL

FDA distribution: “Products were distributed in IL, IN, KY and OH.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Illinois, Indiana, Kentucky, Ohio.

Recall timeline

FDA terminated this recall 5 months after the firm started it.

1. Firm started the recall: Feb 16, 201812. FDA classified it Class II: Mar 8, 201823. Published in FDA’s Enforcement Report: Mar 14, 201834. FDA terminated the recall: Jul 11, 201842018
  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-0908-2018 (February 16, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0908-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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