Stracciatella Gelato (Bonta) – undeclared soy (2023)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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,
Brand
Bonta - Natural Artisan Gelato LLC
Lot Codes / Batch Numbers
1 pint and half-gallon container is marked with code 23298 and are best by October 25, 2024.
Products Sold
1 pint and half-gallon container is marked with code 23298 and are best by October 25, 2024.
Bonta - Natural Artisan Gelato LLC is recalling Bonta Natural Artisan Gelato Stracciatella is frozen dessert, packaged in blue cardboard pint cups ( due to undeclared soy lecithin.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
undeclared soy lecithin.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IN, OR
Page updated: Jan 6, 2026