Dinstuhl's Pecan Brittle, NET WT 4 oz. (113g), individually packaged in cellophane bags; Ingredients: Sugar, Pecans, Cor
Summary
The FDA issued a Class II for Dinstuhl's Pecan Brittle, NET WT 4 oz. (113g), individually packaged in cellopha by Dinstuhl's Fine Candy Company, Inc.. Reason: Undeclared allergen (milk).
Details
Source
Food Recall
External ID
F-0751-2025
Action Date
2025-05-07
Status
Terminated
Category
food
Product Description
Dinstuhl's Pecan Brittle, NET WT 4 oz. (113g), individually packaged in cellophane bags; Ingredients: Sugar, Pecans, Corn Syrup, Butter, Baking Soda, Salt, Vanilla.
Lot/Code Info: UPC: 7 68050 00755 3; Best by: 06-15-25; Batch number: R15; Product number: 00755
Quantity Affected: 12 units
Reason for Recall
Undeclared allergen (milk)
Distribution
Three (3) retailers in MO and MS
Type: Voluntary: Firm initiated
Recall Initiated: 2025-03-04
Company
Memphis, TN
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 34 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Dinstuhl's Fine Candy Company, Inc. has 3 FDA actions in our database, including 3 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 (Dinstuhl's Fine Candy Company, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Dinstuhl's Fine Candy Company, Inc. have FDA actions?
Dinstuhl's Fine Candy Company, Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0751-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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