Harris Teeter Recall: The firm was notified by their contract manufacture that the product contains undeclared hazelnuts.

🇺🇸 United States

1. March 26, 2021 - Recall initiated
2. April 21, 2021 - Reported by source
3. August 26, 2021 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0428-2021

Event ID

87629

Status

Terminated

Classification

Class I

Company

Harris Teeter

Product description

HARRIS TEETER FRESH FOODS MARKET 3 Layer COOKIES & CREME CAKE NET WT 48 OZ (3 LB) 1.36kg packages PROUDLY DISTRIBUTED BY: HARRIS TEETER, LLC MATTHEWS, NC 28105 UPC: 0 72036 95224 0

Quantity

4,378 Whole Cakes

Reason

The firm was notified by their contract manufacture that the product contains undeclared hazelnuts.

Recall initiation date

March 26, 2021

Report date

April 21, 2021

Classification date

Not published in this source record

Termination date

August 26, 2021

Distribution pattern

Product was shipped to the following states: DE, FL, GA, MD, NC, SC, VA & The District of Columbia.

UPC, lot, and code information

Production date, Lot Code: 12/21/2020 1001686863 1/7/2020 1001718406 2/3/2020 1001755913 2/4/2021 1001755914

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Harris Teeter

Other recalls from Harris Teeter

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
Delaware	1
Florida	1
Georgia	1
Maryland	1
North Carolina	1
South Carolina	1
Virginia	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 I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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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