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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Food
Food & Beverages/Packaged & Processed

The Father's Table, LLC: Cheesecake has incorrect rear label. The rear label is for Pumpkin Swirl Cheesecake which lacks peanut allergen declaration.

Agency Publication Date: June 2, 2017
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Summary

The Father's Table, LLC has recalled 425 cases of Denali 'Original' Moose Tracks Cheesecake (18 oz) sold in Florida and Georgia. The product features a black plastic base with a clear dome but was mistakenly labeled with the rear nutrition label for Pumpkin Swirl Cheesecake. This labeling error means the presence of peanuts is not declared on the packaging.

Risk

The product contains peanuts, which are not listed on the back label. This poses a serious risk of a life-threatening allergic reaction for individuals with a peanut allergy if they consume the cheesecake.

What You Should Do

  1. Check your refrigerator for 'Denali Original Moose Tracks Cheesecake' in 18 oz (510g) packages with a black plastic base and clear dome.
  2. Verify if your product is affected by looking for Lot codes 1111711 or 1121731, an Expiration Date of 04/22/2018, and UPC 0-10374-18123-6.
  3. Inspect the rear label; if it describes 'Pumpkin Swirl Cheesecake' instead of Moose Tracks, it is part of the recall.
  4. If you have a peanut allergy, do not consume this product.
  5. Contact The Father's Table, LLC or the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for specific instructions on disposal or potential refunds.

Affected Products

Product: Denali "Original" Moose Tracks Cheesecake (18 oz / 510g)
UPC Codes:
010374181236
Lot Numbers:
1111711/1121731 (Exp 04/22/2018)
Date Ranges: 04/22/2018

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 77225
Status: Active
Manufacturer: The Father's Table, LLC
Manufactured In: United States
Units Affected: 425 cases (9 units per case)

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.