Food Recall Check
Class I · High risk Terminated Initiated Aug 2, 2024 (2 years ago)

Yummy brand Swirly Ices Fruity Melon flavor recall

Recalled by Paradise Distributors, LLC · Edison, NJ, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Undeclared milk.

Undeclared allergen: Milk

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Yummy brand Swirly Ices Fruity Melon flavor Net Wt. 2.3 ounces (65g)x 8 popsicles, Total Net Wt. 18.34 ounces (520g) UPC:734690007536 Also packaged in 30 count packs

Quantity: 268 boxes

Food: Fresh fruit

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.

Lot numbers: 68/2 and 69/1 Expiration dates: 5/28/2026 and 5/30/2026.

Where it was sold

California Florida Iowa Illinois Maryland Michigan New Jersey New York Ohio

FDA's distribution note: Retail supermarkets in CA, NY, IL, FL, MD, NJ, OH, IA, and MI.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. 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
Paradise Distributors, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 2, 2024
In FDA report of
Sep 4, 2024
Terminated
Feb 7, 2025
FDA recall number
F-1791-2024 · event 95123
Official record
FDA enforcement report search

Also recalled with it (4 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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