4 J's Treats, LLC dba Bruttles Gourmet Candies Recall: The Butter Toffee, 16oz box, declares butter but does not declare milk. Label does not declare soy which is present in the non-stick spray being used on the Butter Toffee production trays. The Butter Toffee, 4oz part of the SAMPLERS package, declares butter but does not declare milk, and it does not declare soy which is present in the non-stick spray being used on the Butter Toffee production trays.
United States
TerminatedClass II
- Company
- 4 J's Treats, LLC dba Bruttles Gourmet Candies
- Product
- Butter Toffee, net wt. 16 oz, 6 units per case. Label declar…
- Recall date
- February 28, 2023
- Terminated
- March 23, 2023
- Source
- FDA
Reason for recall
The Butter Toffee, 16oz box, declares butter but does not declare milk. Label does not declare soy which is present in the non-stick spray being used on the Butter Toffee production trays. The Butter Toffee, 4oz part of the SAMPLERS package, declares butter but does not declare milk, and it does not declare soy which is present in the non-stick spray being used on the Butter Toffee production trays.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Butter Toffee, net wt. 16 oz, 6 units per case. Label declares: Butter Toffee, Butter, Sugar, Corn Syrup, Almonds, Vanilla, Salt. www.bruttles.com. Butter Toffee, net wt. 4oz., part of Medium Samplers package. Product is packaged in cello bag and labeled Butter Toffee. Label declares: Butter Toffee, Butter, Sugar, Corn Syrup, Almonds, Vanilla, Salt. www.bruttles.com. | Not published in this source record | 25 boxes of Butter Toffee. 120 boxes of Samplers. | None |
Distribution
- distributed in Washington
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0647-2023
- Event ID
- 91828
- Status
- Terminated
- Classification
- Class II
- Company
- 4 J's Treats, LLC dba Bruttles Gourmet Candies
- Product description
- Butter Toffee, net wt. 16 oz, 6 units per case. Label declares: Butter Toffee, Butter, Sugar, Corn Syrup, Almonds, Vanilla, Salt. www.bruttles.com. Butter Toffee, net wt. 4oz., part of Medium Samplers package. Product is packaged in cello bag and labeled Butter Toffee. Label declares: Butter Toffee, Butter, Sugar, Corn Syrup, Almonds, Vanilla, Salt. www.bruttles.com.
- Quantity
- 25 boxes of Butter Toffee. 120 boxes of Samplers.
- Reason
- The Butter Toffee, 16oz box, declares butter but does not declare milk. Label does not declare soy which is present in the non-stick spray being used on the Butter Toffee production trays. The Butter Toffee, 4oz part of the SAMPLERS package, declares butter but does not declare milk, and it does not declare soy which is present in the non-stick spray being used on the Butter Toffee production trays.
- Recall initiation date
- February 28, 2023
- Report date
- March 29, 2023
- Classification date
- Not published in this source record
- Termination date
- March 23, 2023
- Distribution pattern
- distributed in Washington
- UPC, lot, and code information
- None
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: 4 J's Treats, LLC dba Bruttles Gourmet Candies
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
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Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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?
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