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Cheesecake Royale, Inc. 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.

United States

TerminatedClass II

Company
Cheesecake Royale, Inc.
Product
Bake-a-holic Pecan Bars Cheesecake Royale Pecan Bars
Recall date
June 17, 2025
Terminated
February 25, 2026
Source
FDA

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.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Bake-a-holic Pecan Bars Cheesecake Royale Pecan Bars Not published in this source record 60 cases - 48 pieces per case tba

Distribution

  • Texas

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-0602-2025
Event ID
97108
Status
Terminated
Classification
Class II
Company
Cheesecake Royale, Inc.
Product description
Bake-a-holic Pecan Bars Cheesecake Royale Pecan Bars
Quantity
60 cases - 48 pieces per case
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 listed in Contains statement. Further review of label revealed "soy" had been removed.
Recall initiation date
June 17, 2025
Report date
September 24, 2025
Classification date
Not published in this source record
Termination date
February 25, 2026
Distribution pattern
Texas
UPC, lot, and code information
tba
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Cheesecake Royale, Inc.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.