Bonta - Natural Artisan Gelato LLC Recall: undeclared soy lecithin.
United States
TerminatedClass II
- Company
- Bonta - Natural Artisan Gelato LLC
- Product
- Bonta Natural Artisan Gelato Stracciatella is frozen dessert…
- Recall date
- November 9, 2023
- Terminated
- December 7, 2023
- Source
- FDA
Reason for recall
undeclared soy lecithin.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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." | Not published in this source record | 1 pint container = 20. Half-Gallon container = 4 | 1 pint and half-gallon container is marked with code 23298 and are best by October 25, 2024. |
Distribution
- Distributed in Bend (Oregon)
- Redmond (Oregon)
- Sisters (Oregon)
- Tumalo (Oregon)
- and Terrebonne (Oregon).
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0468-2024
- Event ID
- 93425
- Status
- Terminated
- Classification
- Class II
- Company
- Bonta - Natural Artisan Gelato LLC
- 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."
- Quantity
- 1 pint container = 20. Half-Gallon container = 4
- Reason
- undeclared soy lecithin.
- Recall initiation date
- November 9, 2023
- Report date
- December 6, 2023
- Classification date
- Not published in this source record
- Termination date
- December 7, 2023
- Distribution pattern
- Distributed in Bend (Oregon), Redmond (Oregon), Sisters (Oregon), Tumalo (Oregon), and Terrebonne (Oregon).
- UPC, lot, and code information
- 1 pint and half-gallon container is marked with code 23298 and are best by October 25, 2024.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Bonta - Natural Artisan Gelato LLC
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
