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CriticalFDAfda-F-1791-2022UNDECLARED ALLERGEN

1.5 quarts (1.41 L) Chocolate to Die For Premium Ice Cream UPC: 83057 17049 Plant Code 29-050

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
3,222
Recall Date
July 12, 2022
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1791-2022.

The product may contain undeclared peanuts.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1791-2022.

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 Belfonte Ice Cream & Dairy Foods Co 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-1791-2022.

Belfonte Ice Cream & Dairy Foods Co

FDA

About the U.S. Food and Drug Administration

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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Belfonte Ice Cream & Dairy Foods Co Recall FAQ

Belfonte Ice Cream & Dairy Foods Co is the subject of a dairy safety report: 1.5 quarts (1.41 L) Chocolate to Die For Premium Ice Cream UPC: 83057 17049 Plant Code 29-050. The notice was published on July 12, 2022 by the U.S. Food and Drug Administration (FDA). Approximately 3,222 units are potentially affected.