Class IITerminated in FDA datasetNov 9, 2023

Bonta Natural Artisan Gelato Stracciatella is frozen dessert, packaged in blue cardboard pint cups (

Recalling firm: Bonta - Natural Artisan Gelato LLC

Why it was recalled

undeclared soy lecithin.

Check the codes ↓

The exact 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, 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."

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

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Original FDA code information

1 pint and half-gallon container is marked with code 23298 and are best by October 25, 2024.

TypeCode / valueContext
best byOctober 25, 20241 pint and half-gallon container is marked with code 23298 and are best by October 25, 2024.

Recall details

Recall number
F-0468-2024
Event ID
93425
FDA status
Terminated
Initiated
Nov 9, 2023
Reported
Dec 6, 2023
Classified
Nov 28, 2023
Terminated
Dec 7, 2023
Quantity
1 pint container = 20. Half-Gallon container = 4
Location
Bend, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Distributed in Bend (Oregon), Redmond (Oregon), Sisters (Oregon), Tumalo (Oregon), and Terrebonne (Oregon).

FDA source record · F-0468-2024

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.