Belgian Yummies Homemade Ice Cream Birthday Cake Gelato. Packaged in 5 Liter gray carapina liner.
Summary
The FDA issued a Class II for Belgian Yummies Homemade Ice Cream Birthday Cake Gelato. Packaged in 5 Liter g by Belgian Yummies. Reason: Undeclared Allergen: Yellow #5.
Details
Source
Food Recall
External ID
F-1229-2024
Action Date
2024-05-15
Status
Terminated
Category
food
Product Description
Belgian Yummies Homemade Ice Cream Birthday Cake Gelato. Packaged in 5 Liter gray carapina liner.
Lot/Code Info: No lot numbers provided; Expiration date is 6 months from production date.
Quantity Affected: 31
Reason for Recall
Undeclared Allergen: Yellow #5
Distribution
The products were only distributed in the state of Florida.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-03-20
Company
Fort Myers, FL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Belgian Yummies has 9 FDA actions in our database, including 9 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Belgian Yummies) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Belgian Yummies have FDA actions?
Belgian Yummies has 9 FDA actions in our database, including 9 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1229-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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