RECALL RECORD — CLASS IRecall closedF-0383-2017/FDA enforcement
Bindi North America·Food·Oct 13, 2016

Bindi Fantasia Nel Dessert, 7982 Coconut Gran Sorbetto, 1.24 Gal (4.8l)

What you need to know

Class I
  • What happened

    Product recalled due to undeclared milk allergen (sodium caseinate).

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall closed · classified by the FDANJ, NYMore food

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Product identification

Source: FDA FOOD

Brand nameBindi North America
Recalling firmBindi North AmericaBelleville, NJ, United States
UPC / barcodes
8 15073 01326 6
Lot / date codes
  • Lot #6211 with best before date 07/29/18 and Lot #6265 with best before date 09/21/18
Distribution area
NJNY

NJ and NY

United States

Quantity affected27 cases (Lot #6211) and 6 cases (Lot #6265)
Recall initiationFDA report date: November 16, 2016
FDA recall numberF-0383-2017

Beyond the headline

The recall, in context

Bindi North America initiated this food recall on October 13, 2016. The FDA enforcement report states: Product recalled due to undeclared milk allergen (sodium caseinate). The FDA report lists distribution as: NJ and NY.

The FDA enforcement report describes the reason as: Product recalled due to undeclared milk allergen (sodium caseinate).

Bindi Fantasia Nel Dessert, 7982 Coconut Gran Sorbetto, 1.24 Gal (4.8l) was made or distributed by Bindi North America in Belleville, NJ, United States. This page reflects FDA report F-0383-2017, dated November 16, 2016.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared milk

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a milk allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed cow's milk allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a milk allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Bindi Fantasia Nel Dessert, 7982 Coconut Gran Sorbetto, 1.24 Gal (4.8l) recall?

Bindi North America recalled Bindi Fantasia Nel Dessert, 7982 Coconut Gran Sorbetto, 1.24 Gal (4.8l) in an FDA Class I enforcement action reported as F-0383-2017. Product recalled due to undeclared milk allergen (sodium caseinate).

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have a milk allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Bindi North America recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0383-2017. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Bindi North America

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.