All Ice Cream and Ice Cream products within expiry; manufactured by Royal Ice...
FDA Recall #F-0863-2022 — Class I — February 1, 2022
Recall Summary
| Recall Number | F-0863-2022 |
| Date Initiated | February 1, 2022 |
| Classification | Class I |
| Status | Terminated |
| Type | Voluntary: Firm initiated |
| Product Type | Food |
Recalling Firm
| Firm | The Royal Ice Cream Company Inc. |
| Location | Manchester, CT |
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
Reason for Recall
Product may be contaminated with Listeria monocytogenes.
Classification
Class I — A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Distribution Pattern
MA, CT, RI, VT, NY, LA, FL, TX, NH, WI, PA, GA, NJ, MN, ME, MD, AZ, MI, NC, SC, OH
Product Quantity
90 sleeves
Product Codes / Lot Numbers
All product within expiry (all product that is not currently expired is affected by the recall).
What Should You Do?
Stop consuming this product immediately. Check your home for the recalled item and dispose of it safely. If you experienced a health issue after consuming this product, contact your doctor and report it to the FDA MedWatch.
Frequently Asked Questions
Stop consuming the product immediately and do not donate or give it to others. Check the recall notice above for specific disposal or return instructions. Many food recalls ask you to throw the product away and retain the packaging for a possible refund from the retailer. If you purchased it online, check your order history — some retailers send recall notifications directly to customers. You do not need a receipt to report an issue or seek a refund; the fact of purchase is typically sufficient.
Listeria monocytogenes is one of the most serious foodborne pathogens. Unlike most bacteria, Listeria can grow at refrigerator temperatures (below 40°F), meaning refrigerating a contaminated product does not stop the risk. Symptoms can appear 1 to 4 weeks after eating contaminated food and may include fever, muscle aches, headache, stiff neck, confusion, and loss of balance. Listeriosis is particularly dangerous for pregnant women — infection can cause miscarriage, stillbirth, or premature delivery. If you consumed this recalled product and are in a high-risk group (pregnant, elderly, or immunocompromised), contact your doctor immediately even if you feel well.
Report foodborne illnesses and adverse food reactions to the FDA through the MedWatch Safety Reporting Portal at FDA.gov, or by calling 1-800-332-1088. You can also report issues directly to the FDA's Safety Reporting Portal at SafetyReporting.hhs.gov. If you believe there is an immediate public health risk, contact your local health department. Your report helps the FDA identify contamination patterns, initiate recalls faster, and protect other consumers from the same hazard. Include as much detail as possible: the product name, lot code, purchase date and location, and a description of your symptoms or findings.
The FDA assigns a status to each recall action throughout its lifecycle. "Ongoing" means the recall is active — the firm is still working to remove the product from commerce and notify consumers. "Completed" means the recall strategy has been implemented and the FDA has determined that the recalling firm has taken all appropriate steps to remove the product. "Terminated" means the FDA has reviewed the results and concluded the recall is complete. Even if a recall is marked as completed or terminated, you should still discard any recalled products you find at home — the recall status refers to the firm's compliance actions, not the safety of product still in consumers' possession.