Yummy brand Swirly Ices Assorted Flavors Net Wt. 2.3 ounces (65g)x 8 popsicles, Total Net Wt. 18.34 ounces (520g) UPC: 7
Summary
The FDA issued a Class I for Yummy brand Swirly Ices Assorted Flavors Net Wt. 2.3 ounces (65g)x 8 popsicles, by PARADISE DISTRIBUTORS, LLC. Reason: Undeclared milk..
Details
Source
Food Recall
External ID
F-1793-2024
Action Date
2024-09-04
Status
Terminated
Category
food
Product Description
Yummy brand Swirly Ices Assorted Flavors Net Wt. 2.3 ounces (65g)x 8 popsicles, Total Net Wt. 18.34 ounces (520g) UPC: 734690007574. Contains Fruity Melon, Churning Cherry, Berry Blast, and Tropical Tornado flavored popsicles
Lot/Code Info: Lot numbers: 68/2 and 69/1 Expiration dates: 5/28/2026 and 5/30/2026.
Quantity Affected: 282 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
Company
Edison, NJ
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-1793-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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