Regal Food Inc./dba The Pizza Shop Recall: FDA inspection found that allergen sub ingredients are not declared on the label - wheat, soy, milk.

🇺🇸 United States

1. May 15, 2019 - Recall initiated
2. June 26, 2019 - Reported by source
3. November 19, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1459-2019

Event ID

82877

Status

Terminated

Classification

Class II

Company

Regal Food Inc./dba The Pizza Shop

Product description

Regal's Fundraising Cookies: Cornflake flavor. Net Weight 12 oz. (340 grams). All varieties have the same ingredient list: Flour, Sugar, Cotton Seed Oil, Butter Blend, Chocolate Chips, Salted Butter, Vanilla Extract, Salt, Baking Soda. Regal Foods, Honolulu, HI www.regalfoodsusa.com

Quantity

N/A

Reason

FDA inspection found that allergen sub ingredients are not declared on the label - wheat, soy, milk.

Recall initiation date

May 15, 2019

Report date

June 26, 2019

Classification date

Not published in this source record

Termination date

November 19, 2019

Distribution pattern

HI only - island of Oahu

UPC, lot, and code information

all manufacturing codes - i.e.05/02/19

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 82877 with 2 other product entries in Public Health Trace.

Responsible company: Regal Food Inc./dba The Pizza Shop

Other recalls from Regal Food Inc./dba The Pizza Shop

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Hawaii	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

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: July 18, 2026 ET

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.

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