Recall record at a glance
| Official record | F-0863-2022 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | The Royal Ice Cream Company Inc. |
| Report date | Mar 23, 2022 |
| Recall initiation date | Feb 1, 2022 |
| Quantity | 90 sleeves |
| Location | Manchester, CT, United States |
Official product description
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
Why the product was recalled
Product may be contaminated with Listeria monocytogenes.
Distribution information
MA, CT, RI, VT, NY, LA, FL, TX, NH, WI, PA, GA, NJ, MN, ME, MD, AZ, MI, NC, SC, OH
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Telephone.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.