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The Royal Ice Cream Company Inc.
FDA recall F-0863-2022 · Class I · reported 2022-03-23 · Terminated
- Product
- All Ice Cream and Ice Cream products within expiry; manufactured by Royal Ice Cream Company; manufactured in Manchester, CT; all effected products will have the manufacturing plant number "CT121" or "CT #121"; RETAIL BRANDS EFFECTED: Batch brand pints, all flavors; Royal Ice Cream brand half gallons, pints, cakes, all specialties; Ronny Brook Ice Cream all flavor pints & 3 gallon tubs; New Orleans Ice Cream all flavor pints & 2.5-gallon tubs; Maple Valley Ice Cream all flavor pints; Art Cream all pint flavors; Sweet Scoops Yogurt all pint Flavors; Gelato Fiasco all pint Flavors; Biggy Iggy's Ice Cream Sandwiches; Munson Chip Wich Ice Cream sandwiches; Giffords Ice Cream Sandwiches all flavors; Chewy Louie Ice Cream Sandwiches; Snow Wich Ice Cream Sandwich; Newport Creamery - crazy vanilla, Vanilla & Chocolate, Vanilla & Coffee HG only; Dough Wich - Conn. 4 oz Cookie Dough Sandwich in all flavors of vanilla, chocolate, and french vanilla; Doris Italian Markets - Florida - Spumoni wedge, Spumoni Half Gallon, Tartufo, Cannoli, Spumoni pie slices; Highland Park Market brand ice cream, all sizes and all flavors; Labriola's Italian Stores, Spumoni Ice Cream, 64 ounces. FOOD SERVICE ONLY BRANDS EFFECTED: Cronin's brand; Orfitelli brand; Royal Ice Cream Company; Delicious Desserts Inc. brand; Sweet Service brand; Desserts Plus brand
- Reason
- Product may be contaminated with Listeria monocytogenes.
- Quantity
- 90 sleeves
- Distribution
- MA, CT, RI, VT, NY, LA, FL, TX, NH, WI, PA, GA, NJ, MN, ME, MD, AZ, MI, NC, SC, OH
- Firm location
- CT, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Telephone
- Recall started
- 2022-02-01
- Terminated
- 2023-08-21
- Code info
- All product within expiry (all product that is not currently expired is affected by the recall).
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.