FDA recall record

PARADISE DISTRIBUTORS Yummy brand Swirly Ices Churning Cherry flavor Net Wt recall — FDA F-1792-2024

Undeclared milk.

Class Iclassification
F-1792-2024official record ID
Sep 4, 2024report date

Recall record at a glance

Official recordF-1792-2024
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmPARADISE DISTRIBUTORS, LLC
Report dateSep 4, 2024
Recall initiation dateAug 2, 2024
Quantity310 boxes
LocationEdison, NJ, United States

Official product description

Yummy brand Swirly Ices Churning Cherry flavor Net Wt. 2.3 ounces (65g)x 8 popsicles, Total Net Wt. 18.34 ounces (520g) UPC:734690007543 Also packaged in 30 count packs

Why the product was recalled

Undeclared milk.

Distribution information

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

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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