CLASS II Food recall · Reported 14 Nov 2018 · FDA Enforcement Report

Tropical Dreams Super Premium Ice Cream Vegan Coconut recalled

Edney and Sellers is recalling Tropical Dreams Super Premium Ice Cream Vegan Coconut, distributed in Hawaii. The recall was initiated on 19 Oct 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll lot numbers up to 625305
Quantity recalled28 cases - 8 pints per case

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0369-2019
FDA event ID
81363
Recalling firm
Edney and Sellers, Kamuela, HI
Classification
Class II
Status
Terminated
Recall initiated
19 Oct 2018
FDA classified
6 Nov 2018
Reported
14 Nov 2018
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Soy

Timeline

19 Oct 2018Recall initiated by company
6 Nov 2018Classified by FDA+18 days
14 Nov 2018Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

Tropical Dreams Super Premium Ice Cream Vegan Coconut; Pint container; UPC: 7 66150 09985 0 Ingredients: Coconut milk, organic sugar, carob bean gum and guar gum (stabilizer), dextrose. Food Allergy warning: This product was prepared at facilities where milk, eggs, wheat, peanuts, tree nuts and chocolate were processed.

Where it was distributed

HI only

Hawaii

Questions about this recall

Why was it recalled?

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

Which lots are affected?

All lot numbers up to 625305

Where was it sold?

HI only

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 81363

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