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FDA source record Class II Terminated

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). ...

Recall Date: 2023-11-09 Recalling Firm: Bonta - Natural Artisan Gelato LLC Record Ref: F-0468-2024

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns 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). ... and names Bonta - Natural Artisan Gelato LLC as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Bonta - Natural Artisan Gelato LLC
  • Classification: Class II
  • Status: Terminated
  • Recall date: 2023-11-09
Best identifiers to check for a FDA record

Compare UPC/GTIN, lot or batch code, package size, flavor or variety, and any best-by/use-by date listed in the notice.

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Product Description & Identification

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."

Reason for Recall / Hazard Identified

undeclared soy lecithin.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

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

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-0468-2024
Indexed update
2026-08-09 21:59:13 UTC
Official source
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