Summary
The FDA issued a Class II for Bake-a-holic Pecan Bars Cheesecake Royale Pecan Bars by Cheesecake Royale, Inc.. Reason: Review of Label determined allergen was listed as unsalted butter/ heavy cream. In one instance of identified label, there was no milk or dairy listed.
Details
Source
Food Recall
External ID
H-0602-2025
Action Date
2025-09-24
Status
Terminated
Category
food
Product Description
Bake-a-holic Pecan Bars Cheesecake Royale Pecan Bars
Lot/Code Info: tba
Quantity Affected: 60 cases - 48 pieces per case
Reason for Recall
Review of Label determined allergen was listed as unsalted butter/ heavy cream. In one instance of identified label, there was no milk or dairy listed listed in Contains statement. Further review of label revealed "soy" had been removed.
Distribution
Texas
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-17
Company
Dallas, TX
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 51 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 (Cheesecake Royale, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Cheesecake Royale, Inc. have FDA actions?
This is the only FDA action we have on record for Cheesecake Royale, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0602-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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