Class IITerminated in FDA datasetOct 19, 2018

Tropical Dreams Super Premium Ice Cream Chocolate Coconut Macadamia Nut; Pint container

Recalling firm: Edney and Sellers, Ltd.

Why it was recalled

During FDA inspection it was found that soy oil and coconut was not declared on package label.

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Compare the exact product and package details with the label you have.

ProductTropical Dreams Super Premium Ice Cream Chocolate Coconut Macadamia Nut; Pint container; UPC 7 18122 41477 2 Ingredients: Cream, Sugar, Skim milk powder, water, cocoa powder, dark chocolate, pure vanilla, macadamia nuts, corn syrup, barley malt, carob bean gum and guar gum (stabilizer) dextrose, natural flavorings, caramel color, citric acid, soy lecithin, propylene glycol, gum zanthan, gum Arabic Food Allergy warning: This product was prepared at facilities where milk, eggs, wheat, peanuts, tree nuts and chocolate were processed.
UPC718122414772

FDA code information

All lot numbers up to 625305

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Tropical Dreams Super Premium Ice Cream Chocolate Coconut Macadamia Nut; Pint container; UPC 7 18122 41477 2 Ingredients: Cream, Sugar, Skim milk powder, water, cocoa powder, dark chocolate, pure vanilla, macadamia nuts, corn syrup, barley malt, carob bean gum and guar gum (stabilizer) dextrose, natural flavorings, caramel color, citric acid, soy lecithin, propylene glycol, gum zanthan, gum Arabic Food Allergy warning: This product was prepared at facilities where milk, eggs, wheat, peanuts, tree nuts and chocolate were processed.

Extracted codes and context

TypeCode / valueContext
UPC718122414772s Super Premium Ice Cream Chocolate Coconut Macadamia Nut; Pint container; UPC 7 18122 41477 2 Ingredients: Cream, Sugar, Skim milk powder, water, cocoa powder, dark chocolate, pure vanilla, macadamia nuts, corn

Recall details

Recall number
F-0366-2019
Event ID
81363
FDA status
Terminated
Initiated
Oct 19, 2018
Reported
Nov 14, 2018
Classified
Nov 6, 2018
Terminated
Dec 17, 2018
Quantity
225 cases - 8 pints per case
Location
Kamuela, HI, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

HI only

FDA source record · F-0366-2019

Data updated September 16, 2026. View official FDA data ↗

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