Quality Dairy Farms Mercer's brand 6 ICE CREAM SANDWICHES TO GO recall — FDA H-1343-2026

Recall record at a glance

Official product description

Mercer's brand 6 ICE CREAM SANDWICHES TO GO; packaged in clear plastic; ice cream sandwiches may be rolled in peanuts which are visible through product packaging Ingredients: Cream, sugar, nonfat milk, whey, cocoa (alkalized), stabilizer (guar gum, carrageenan), chocolate wafer (wheat flour, sugar, high fructose corn syrup, shortening [partially hydrogenated soybean oil], caramel color, soy flour, corn starch, baking soda, soy lecithin, cocoa, salt, natural vanilla flavor) and/or chocolate chip cookie (Enriched wheat flour [wheat flour, niacin, reduced iron, thiamine, riboflavin, folic acid], palm oil, sugar, chocolate chips [sugar, chocolate liquor, cocoa butter, dextrose, soy lecithin], brown sugar, containers 2% or less of dextrose, salt, leavenings [ammonium bicarbonate, baking soda, sodium acid pyrophosphate], natural flavor) and/or Oreo cookie (unbleached enriched flour (wheat flour, niacin, reduced iron, thiamine mononitrate [vitamin B1], riboflavin [vitamin B2], folic acid), sugar, canola oil, cocoa [processed with alkali], high fructose corn syrup, leavening [baking soda and/or calcium phosphate], salt, soy lecithin, chocolate, artificial flavor. May contain nuts. May contain Chocolate Sprinkles (sugar, hydrogenated palm kernel oil, cocoa powder (processed with alkali), corn starch, maltodextrin, cellulose gum, sunflower lecithin, natural and artificial flavor, carnauba wax, vanillin) May contain Carnival Sprinkles (sugar, hydrogenated palm kernel oil, corn starch, sunflower lecithin, FD&C colors (Yellow #6 Lake, Yellow #5 Lake, Blue #1 Lake, Red #40 Lake, Red #3 Dye) maltodextrin, cellulose gum, carnauba wax, vanillin) Plant #: 36-5692. Boonville, NY net weight 1.5lb

Why the product was recalled

Undeclared peanuts

Distribution information

NY

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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

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