Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 4, 2019 (7 years ago)

Lalamilo Farms Tropical Dreams Hawaiian Ice Cream recall

Recalled by Edney and Sellers, Ltd. · Kamuela, HI, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Firm received report of consumer finding plastic pieces, approximately 1 inch in length, in their Strawberry Cheesecake Ice Cream.

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

Lalamilo Farms Tropical Dreams Hawaiian Ice Cream - Strawberry Cheesecake. Sold in 3 gallon tubs, 1.5 gallon tubs, 5 L tubs, 8 oz. cups. Ingredients: Cream, Nonfat Milk, Sugar, Corn Syrup, Water, High Fructose Corn Syrup, Cream Cheese Powder {Cream Cheese{milk, culture, salt, Carob Bean Gum, Enzyme}, Nonfat Milk], Strawberries, Modified Cornstarch, Citric Acid, Salt, Guar Sum and Carob Bean Gum, Xanthan Gum, Natural and Artificial Flavors, Red 40, Blue 1, Sodium Benzoate, Sodium Alginate. Contains: Milk Manufactured by Tropical Dreams Ice Cream, 66-1250 Laiamilo Farm Road, Kamuela, HI 96743

Quantity: 3 gal - 188; 1.5 gal - 199; 5 L - 8; 8 oz. cups - 950

Food: Cheese Ice cream Berries

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

All lot numbers up to #625579

Where it was sold

California

FDA's distribution note: Hi and CA

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Edney and Sellers, Ltd.
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 4, 2019
In FDA report of
Dec 18, 2019
Terminated
Feb 21, 2020
FDA recall number
F-0305-2020 · event 84432
Official record
FDA enforcement report search

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