CLASS I Food recall · Reported 4 Sep 2024 · FDA Enforcement Report

Yummy Swirly Ices Fruity Melon flavor recalled by Paradise Distributors

Paradise Distributors is recalling Yummy Swirly Ices Fruity Melon flavor, distributed in 9 states. The recall was initiated on 2 Aug 2024 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot numbers: 68/2 and 69/1 Expiration dates: 5/28/2026 and 5/30/2026.
Quantity recalled268 boxes

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-1791-2024
FDA event ID
95123
Recalling firm
Paradise Distributors, Edison, NJ
Brand
Yummy
Classification
Class I
Status
Terminated
Recall initiated
2 Aug 2024
FDA classified
5 Sep 2024
Reported
4 Sep 2024
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Milk

Timeline

2 Aug 2024Recall initiated by company
4 Sep 2024Published in enforcement report+33 days
5 Sep 2024Classified by FDA+1 day

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

Reason for recall

Undeclared milk.

Product as listed by the FDA

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

Where it was distributed

Retail supermarkets in CA, NY, IL, FL, MD, NJ, OH, IA, and MI.

CaliforniaFloridaIowaIllinoisMarylandMichiganNew JerseyNew YorkOhio

Questions about this recall

Why was it recalled?

Undeclared milk.

Which lots are affected?

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

Where was it sold?

Retail supermarkets in CA, NY, IL, FL, MD, NJ, OH, IA, and MI.

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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

4 other products · FDA event 95123

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