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Lower risk Food recall · FDA · Published July 17, 2018

Cracker Barrel Country Candies Fudge Peanut Butter Recall: Incorrect Peanut Label

Cracker Barrel recalls fudge peanut butter products due to incorrect ingredient labeling. Products may contain undeclared peanut butter, posing a risk for allergic individuals. Check packaging for specific batch numbers and contact Cracker Barrel for details.

🇺🇸 FDA recall #F-1762-2018FoodCracker Barrel ›
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Contact the company

Recalling firmCountry Fresh Food & Confections Inc.405 Main St · Oliver Springs, TN 37840-1724
✎ GovInfoNow plain-language explainer

What happened, in plain English

Cracker Barrel is recalling certain fudge peanut butter products because the back panel label incorrectly states the ingredients, potentially hiding peanut butter. This could affect people with peanut allergies who might consume the product without knowing. Read more at govinfonow.com/recall/18949-cracker-barrel-country-candies-fudge-peanut-butter-recall-incorrect-peanut.

Source Summary by GovInfoNow · govinfonow.com/recall/18949-cracker-barrel-country-candies-fudge-peanut-butter-recall-incorrect-peanut · Updated October 6, 2026 · FDA enforcement record: FDA #F-1762-2018

Cite this page

“Cracker Barrel Country Candies Fudge Peanut Butter Recall: Incorrect Peanut Label.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18949-cracker-barrel-country-candies-fudge-peanut-butter-recall-incorrect-peanut. Based on FDA recall #F-1762-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1762-2018%22&limit=1).

Why it’s dangerous

The product's back panel label incorrectly lists ingredients, meaning peanut butter might not be visible to consumers. This could lead to accidental consumption by individuals with peanut allergies who are unaware the product contains peanuts.

Who’s affected

People who own or use the recalled Cracker Barrel fudge peanut butter products are most at risk if they have peanut allergies. The recall affects specific batches sold in Lebanon, Tennessee.

How to tell if you have this one

Check for batch numbers CB11811401, CB118117-05, CB118099-04, or CB118113-02 with best by dates of November 1, 2018, November 6, 2018, September 5, 2018, or October 31, 2018.

  • Brand
    Cracker Barrel
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for batch numbers CB11811401, CB118117-05, CB118099-04, or CB118113-02 with specific best by dates.

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: “Product was distributed one distributor in Tennessee.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Tennessee.

Recall timeline

FDA terminated this recall 7 months after the firm started it.

1. Firm started the recall: Jul 17, 201812. FDA classified it Class II: Aug 7, 201823. Published in FDA’s Enforcement Report: Aug 15, 201834. FDA terminated the recall: Feb 20, 2019420182019
  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-1762-2018 (July 17, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1762-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 6, 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