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Belfonte Ice Cream & Dairy Foods Co

FEI 1930458 · 1511 Brooklyn Ave, Kansas City, Missouri, 64127, United States

Per FDA, as of 2026-10-31 · Sources: FDA Data Dashboard, Import Alerts, Enforcement Reports

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Import alerts
0
Import refusals (5 years)
0
Warning letters
0
Last FDA action
2025-02-20
1 year ago

FDA record

  1. 2022-07-12
    RecallRecall F-1791-2022 · Class 1 · The product may contain undeclared peanuts.
    1.5 quarts (1.41 L) Chocolate to Die For Premium Ice Cream UPC: 83057 17049 Plant Code 29-050
    Source: FDA Enforcement Reports
  2. 2019-08-05
    RecallRecall F-1991-2019 · Class 2 · Undeclared allergens peanuts: Peanut butter ice cream was placed in containers labeled to be frozen vanilla yogurt
    FROZEN VAN YOG, in 3 gallon cardboard buckets
    Source: FDA Enforcement Reports
  3. 2012-10-09
    RecallRecall F-0651-2013 · Class 1 · Products may contain peanut butter base with potentially contaminated with Salmonella.
    Belfonte Home Run Sundae Ice Cream, A Baseball Nut Blend of Chocolate Peanuts, Chocolate Coated Pretzels, and a Thick Fudge Swirl in Peanut Butter/Chocolate Ice Cream, 56 oz. (1.66L) Belonite Ice Cream Company, Kansas City, MO
    Source: FDA Enforcement Reports
  4. 2012-10-09
    RecallRecall F-0652-2013 · Class 1 · Products may contain peanut butter base with potentially contaminated with Salmonella.
    Belfonte Mama's Choice Premium Ice Cream, Reverse Peanut Butter Pie, Peanut Butter Coated Fudge Filled Cups, Peanut Butter Flakes and Swirled Chocolate Cookie Pie Crust Ribbon in Peanut Butter Ice Cream, 56 oz. (1.66L) Belonite Ice Cream Co…
    Source: FDA Enforcement Reports
  5. 2009-02-05
    RecallRecall F-209-9 · Class 1 · The product was manufactured using peanut product recalled by Peanut Corporation of America because it has the potential to be contaminated with Salmonella.
    Belfonte ¿ Gal. Square Home Run Sundae ice cream, UPC 83057-01023-9, with date codes 04/08/2009 and 05/29/2009. The responsible firm is listed on the product label as Belfonte Ice Cream Company, Kansas City, MO 64127.
    Source: FDA Enforcement Reports