English Toffee, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 5oz, packed in flexible plastic bag
Summary
The FDA issued a Class II for English Toffee, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 5oz, by The Candy Barn. Reason: Allergen labeling: specific tree nut (pecans) not listed in the 'contains' statement.
Details
Source
Food Recall
External ID
H-0565-2025
Action Date
2025-09-10
Status
Terminated
Category
food
Product Description
English Toffee, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 5oz, packed in flexible plastic bag
Lot/Code Info: No coding
Quantity Affected: 665 packages Total
Reason for Recall
Allergen labeling: specific tree nut (pecans) not listed in the 'contains' statement
Distribution
Stringtown Grocery, Kalona, IA Golden Delight Bakery, Kalona, IA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-08-06
Company
Riverside, IA
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 42 food recalls issued in the same week, part of 204 food-related FDA actions this month.
The Candy Barn has 9 FDA actions in our database, including 9 recalls.
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 (The Candy Barn) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does The Candy Barn have FDA actions?
The Candy Barn has 9 FDA actions in our database, including 9 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0565-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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