Bonta Natural Artisan Gelato Stracciatella is frozen dessert, packaged in blue cardboard pint cups (UPC 58745 00309) and
Summary
The FDA issued a Class II for Bonta Natural Artisan Gelato Stracciatella is frozen dessert, packaged in blue c by Bonta - Natural Artisan Gelato LLC. Reason: undeclared soy lecithin..
Details
Source
Food Recall
External ID
F-0468-2024
Action Date
2023-12-06
Status
Terminated
Category
food
Product Description
Bonta Natural Artisan Gelato Stracciatella is frozen dessert, packaged in blue cardboard pint cups (UPC 58745 00309) and in green cardboard half-gallon tubs (UPC 58745 00306). The 1 Pint label is read in parts: "Stracciatella Sweet Cream Freckled with crunchy 70% Dark Chocolate. Ingredients: Milk, sugar, cream. Theo dark chocolate (cocoa beans, cane sugar, cocoa butter), skim milk powder, ***coconut oil***CONTAINS: milk, coconut. The Half-Gallon label is read in parts: "Stracciatella ***Milk, sugar, cream, Theo dark chocolate (cocoa beans, cane sugar, cocoa butter), skim milk powder, ***coconut oil***CONTAINS: milk, coconut. Made on shared equipment with milk, egg, wheat, peanuts, soy, coconut, tree nuts."
Lot/Code Info: 1 pint and half-gallon container is marked with code 23298 and are best by October 25, 2024.
Quantity Affected: 1 pint container = 20. Half-Gallon container = 4
Reason for Recall
undeclared soy lecithin.
Distribution
Distributed in Bend (Oregon), Redmond (Oregon), Sisters (Oregon), Tumalo (Oregon), and Terrebonne (Oregon).
Type: Voluntary: Firm initiated
Recall Initiated: 2023-11-09
Company
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 18 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Bonta - Natural Artisan Gelato LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Bonta - Natural Artisan Gelato LLC have FDA actions?
This is the only FDA action we have on record for Bonta - Natural Artisan Gelato LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0468-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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