RecallHawk
Class I Recall

Marabou Sea Salt Chocolate Bar; 185g; yellow plastic packaging and the word 'havvsalt', the Swedish word for "sea salt";

BonBon NYC LLC.

Summary

The FDA issued a Class I for Marabou Sea Salt Chocolate Bar; 185g; yellow plastic packaging and the word 'hav by BonBon NYC LLC.. Reason: Product may contain undeclared almonds, wheat, and nuts..

Details

Source

Food Recall

External ID

F-1818-2024

Action Date

2024-09-25

Status

Terminated

Category

food

Product Description

Marabou Sea Salt Chocolate Bar; 185g; yellow plastic packaging and the word 'havvsalt', the Swedish word for "sea salt"; product is a flat chocolate bar

Lot/Code Info: Dated: 04.09.2024 and 09.11.2024; OUV0134912 and OUV0140643

Quantity Affected: 3 units

Reason for Recall

Product may contain undeclared almonds, wheat, and nuts.

Distribution

New York

Type: Voluntary: Firm initiated

Recall Initiated: 2024-05-08

Company

BonBon NYC LLC.

New York, NY

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 24 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (BonBon NYC LLC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does BonBon NYC LLC. have FDA actions?

This is the only FDA action we have on record for BonBon NYC LLC. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1818-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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