RecallHawk
Class I Recall

Harris Teeter ASIAGO TEXAS TOAST, NET WT 5.0OZ (0.3lb), INGREDIENTS BREAD***CONTAINS WHEAT, UPC 0 72036 95364 3, Harris

Harris Teeter

Summary

The FDA issued a Class I for Harris Teeter ASIAGO TEXAS TOAST, NET WT 5.0OZ (0.3lb), INGREDIENTS BREAD***CONT by Harris Teeter. Reason: Undeclared Milk. During production the firm discovered that the ingredients "cheese and butter" is not listed in the ingredient statement and therefor.

Details

Source

Food Recall

External ID

H-0029-2026

Action Date

2025-10-15

Status

Terminated

Category

food

Product Description

Harris Teeter ASIAGO TEXAS TOAST, NET WT 5.0OZ (0.3lb), INGREDIENTS BREAD***CONTAINS WHEAT, UPC 0 72036 95364 3, Harris Teeter Raleigh, NC

Lot/Code Info: All dates through 9/15/25

Quantity Affected: 295 units

Reason for Recall

Undeclared Milk. During production the firm discovered that the ingredients "cheese and butter" is not listed in the ingredient statement and therefore the allergen milk was not listed in the contain statement.

Distribution

Product was sold in the following states: DC, DE, FL, GA, MD, NC, SC & VA.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-09-11

Company

Harris Teeter

Matthews, NC

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 55 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Harris Teeter has 85 FDA actions in our database, including 85 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (Harris Teeter) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Harris Teeter have FDA actions?

Harris Teeter has 85 FDA actions in our database, including 85 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0029-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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