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High RiskFDAfda-F-1762-2018UNDECLARED ALLERGEN

Cracker Barrel OLD FASHIONED COUNTRY CANDIES KETTLE COOKED FUDGE PEANUT BUTTER, Nutrition Facts***INGREDIENTS: SUGAR, PEANUT BUTTER***PAC...

Category
Units Affected
331
Recall Date
July 17, 2018
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1762-2018.

Failure to declare peanut butter in the ingredients statement. Product has correct top label with incorrect back panel label.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1762-2018.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Country Fresh Food & Confections Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1762-2018.

Country Fresh Food & Confections Inc.

FDA

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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Country Fresh Food & Confections Inc. Recall FAQ

Country Fresh Food & Confections Inc. is the subject of a dairy safety report: Cracker Barrel OLD FASHIONED COUNTRY CANDIES KETTLE COOKED FUDGE PEANUT BUTTER, Nutrition Facts***INGREDIENTS: SUGAR, PEANUT BUTTER***PAC.... The notice was published on July 17, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 331 units are potentially affected.