Butter Toffee, net wt. 16 oz, 6 units per case. Label declares: Butter Toffee, Butter, Sugar, Corn Syrup, Almonds, Vanil
Summary
The FDA issued a Class II for Butter Toffee, net wt. 16 oz, 6 units per case. Label declares: Butter Toffee, B by 4 J's Treats, LLC dba Bruttles Gourmet Candies. 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.
Details
Source
Food Recall
External ID
F-0647-2023
Action Date
2023-03-29
Status
Terminated
Category
food
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.
Lot/Code Info: None
Quantity Affected: 25 boxes of Butter Toffee. 120 boxes of Samplers.
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.
Distribution
distributed in Washington
Type: Voluntary: Firm initiated
Recall Initiated: 2023-02-28
Company
Spokane Valley, WA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 503 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (4 J's Treats, LLC dba Bruttles Gourmet Candies) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does 4 J's Treats, LLC dba Bruttles Gourmet Candies have FDA actions?
This is the only FDA action we have on record for 4 J's Treats, LLC dba Bruttles Gourmet Candies in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0647-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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