FDA recall record

4 J's Treats, LLC dba Bruttles Gourmet Candies Butter Toffee, net wt recall — FDA F-0647-2023

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…

Class IIclassification
F-0647-2023official record ID
Mar 29, 2023report date

Recall record at a glance

Official recordF-0647-2023
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firm4 J's Treats, LLC dba Bruttles Gourmet Candies
Report dateMar 29, 2023
Recall initiation dateFeb 28, 2023
Quantity25 boxes of Butter Toffee. 120 boxes of Samplers.
LocationSpokane Valley, WA, United States

Official 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.

Why the product was recalled

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.

Distribution information

distributed in Washington

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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