BonBon NYC LLC. Recall: Product may contain undeclared almonds, wheat, and nuts.
United States
TerminatedClass I
- Company
- BonBon NYC LLC.
- Product
- Marabou Sea Salt Chocolate Bar; 185g; yellow plastic packagi…
- Recall date
- May 8, 2024
- Terminated
- September 30, 2025
- Source
- FDA
Reason for recall
Product may contain undeclared almonds, wheat, and nuts.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | Not published in this source record | 3 units | Dated: 04.09.2024 and 09.11.2024; OUV0134912 and OUV0140643 |
Distribution
- New York
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1818-2024
- Event ID
- 95091
- Status
- Terminated
- Classification
- Class I
- Company
- BonBon NYC LLC.
- 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
- Quantity
- 3 units
- Reason
- Product may contain undeclared almonds, wheat, and nuts.
- Recall initiation date
- May 8, 2024
- Report date
- September 25, 2024
- Classification date
- Not published in this source record
- Termination date
- September 30, 2025
- Distribution pattern
- New York
- UPC, lot, and code information
- Dated: 04.09.2024 and 09.11.2024; OUV0134912 and OUV0140643
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Other
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: BonBon NYC 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 I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
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.
