Bindi Fantasia nel dessert Coconut Sorbetto Recalled for Undeclared Milk Allergen
Bindi North America recalls 1.24-gallon Coconut Gran Sorbetto due to undeclared milk allergen sodium caseinate. Consumers should check product labels and contact Bindi for details.
Lower-risk recall
Product recalled due to undeclared milk allergen (sodium caseinate).
Contact the company
What happened, in plain English
Bindi North America is recalling a 1.24-gallon coconut sorbetto because it contains an undeclared milk allergen (sodium caseinate). This poses a risk for people with milk allergies who might experience allergic reactions. Read more at govinfonow.com/recall/23007-bindi-fantasia-nel-dessert-coconut-sorbetto-recalled-for-undeclared-milk.
Source Summary by GovInfoNow · govinfonow.com/recall/23007-bindi-fantasia-nel-dessert-coconut-sorbetto-recalled-for-undeclared-milk · Updated October 9, 2026 · FDA enforcement record: FDA #F-0383-2017
Cite this page
“Bindi Fantasia nel dessert Coconut Sorbetto Recalled for Undeclared Milk Allergen.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23007-bindi-fantasia-nel-dessert-coconut-sorbetto-recalled-for-undeclared-milk. Based on FDA recall #F-0383-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0383-2017%22&limit=1).
Why it’s dangerous
The sorbetto contains sodium caseinate, a milk-derived ingredient that is not listed on the label. This can cause allergic reactions in individuals sensitive to milk proteins.
Who’s affected
People with milk allergies who consume this sorbetto could experience allergic reactions. The product is sold in the United States through Bindi North America.
How to tell if you have this one
Check for the product name 'Bindi Fantasia nel dessert, 7982 Coconut Gran Sorbetto' with UPC 8 15073 01326 6. The product was sold in the U.S. with specific lot numbers and best-by dates.
- Brand
Bindi- Product
Bindi Fantasia nel dessert, 7982 Coconut Gran Sorbetto, 1.24 Gal (4.8L), UPC 8 15073 01326 6, Distributed by: Bindi- Category
Food
What to do — step by step
Check Product Label
Look for the product name and UPC code to confirm if it matches the recalled items.
Where it went and when
Where it was distributed
Distributed in New Jersey and New York.
FDA distribution: “NJ and NY” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: New Jersey, New York.
Recall timeline
FDA terminated this recall 8 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
What are the lot numbers for this product?
Lot #6211 with best before date 07/29/18 and Lot #6265 with best before date 09/21/18.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0383-2017 (October 13, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0383-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.