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Stop using now Food recall · FDA · Published June 7, 2016

Dollywood Cajun Mix Recalled Due to Listeria Contamination

Dollywood Cajun Mix in 9oz bags is recalled due to Listeria Monocytogenes contamination. Check your best-by dates and UPC.

🇺🇸 FDA recall #F-2222-2016FoodDollywood ›
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Contact the company

Recalling firmRucker's Makin Batch Candies, Inc.777 East State St. · Bridgeport, IL 62417
✎ GovInfoNow plain-language explainer

What happened, in plain English

Rucker's Makin Batch Candies, Inc. is recalling Dollywood Cajun Mix because the sunflower kernels are contaminated with Listeria Monocytogenes. The product was sold at Dollywood Theme Park in Sevierville, TN. No remedy or return instructions are provided in this record. Read more at govinfonow.com/recall/24092-dollywood-cajun-mix-recalled-due-to-listeria-contamination.

Source Summary by GovInfoNow · govinfonow.com/recall/24092-dollywood-cajun-mix-recalled-due-to-listeria-contamination · Updated October 9, 2026 · FDA enforcement record: FDA #F-2222-2016

Cite this page

“Dollywood Cajun Mix Recalled Due to Listeria Contamination.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/24092-dollywood-cajun-mix-recalled-due-to-listeria-contamination. Based on FDA recall #F-2222-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2222-2016%22&limit=1).

Why it’s dangerous

The sunflower kernels in the mix are contaminated with Listeria Monocytogenes. Ingesting this bacteria can cause serious illness, particularly for vulnerable individuals.

Who’s affected

Anyone who purchased the 9-ounce bags of Dollywood Cajun Mix at Dollywood Theme Park between January 23, 2016, and November 11, 2016. Consumers are at risk of Listeria infection if they consume the contaminated product.

How to tell if you have this one

Look for Dollywood Cajun Mix packaged in a clear 9-ounce plastic bag with a grey sticker label reading "Dollywood Candy Kitchen". Check the UPC code 4 9000 503302 and best-by codes ranging from 1/23/2016 to 11/11/16.

  • Brand
    Dollywood
  • Product
    Dollywood Cajun Mix packaged in a clear 9 ounce plastic bag with grey sticker label reading in part "Dollywood Candy
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the Dollywood Cajun Mix if it matches the description and dates above due to Listeria risk.

  2. Discard or return the item

    The record does not specify a remedy, so you should discard the product or contact the retailer for guidance.

Where it went and when

Where it was distributed

Distributed in Tennessee.

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: yesTNNorth 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: “The firm shipped this product to one retail facility. The retail facility is Dollywood Theme Park, 1130 Wagner Drive, Sevierville, TN 37862. No foreign Consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Tennessee.

Recall timeline

FDA terminated this recall 2.5 years after the firm started it.

1. Firm started the recall: Jun 7, 201612. FDA classified it Class I: Sep 14, 201623. Published in FDA’s Enforcement Report: Sep 21, 201634. FDA terminated the recall: Dec 21, 2018420162018
  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?

It was shipped to and sold at Dollywood Theme Park, 1130 Wagner Drive, Sevierville, TN 37862.

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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-2222-2016 (June 7, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2222-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 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