RecallHawk
Class I Recall

Yummy brand Swirly Ices Berry Blast flavor Net Wt. 2.3 ounces (65g)x 8 popsicles, Total Net Wt. 18.34 ounces (520g) UPC:

PARADISE DISTRIBUTORS, LLC

Summary

The FDA issued a Class I for Yummy brand Swirly Ices Berry Blast flavor Net Wt. 2.3 ounces (65g)x 8 popsicles by PARADISE DISTRIBUTORS, LLC. Reason: Undeclared milk..

Details

Source

Food Recall

External ID

F-1790-2024

Action Date

2024-09-04

Status

Terminated

Category

food

Product Description

Yummy brand Swirly Ices Berry Blast flavor Net Wt. 2.3 ounces (65g)x 8 popsicles, Total Net Wt. 18.34 ounces (520g) UPC: 734690007550 Also packaged in 30 count packs

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

Quantity Affected: 262 boxes

Reason for Recall

Undeclared milk.

Distribution

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

Type: Voluntary: Firm initiated

Recall Initiated: 2024-08-02

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 24 food recalls issued in the same week, part of 204 food-related FDA actions this month.

PARADISE DISTRIBUTORS, LLC has 5 FDA actions in our database, including 5 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (PARADISE DISTRIBUTORS, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does PARADISE DISTRIBUTORS, LLC have FDA actions?

PARADISE DISTRIBUTORS, LLC has 5 FDA actions in our database, including 5 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1790-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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