Giant/Martin's Crunchy Taco Dinner Kit, Net Wt 9.4 OZ (266g), UPC: 068826757516, DISTRIBUTED BY: ADUSA DISTRIBUTION, LLC
Summary
The FDA issued a Class I for Giant/Martin's Crunchy Taco Dinner Kit, Net Wt 9.4 OZ (266g), UPC: 068826757516, by Teasdale Foods, Inc.. Reason: Undeclared allergen - milk.
Details
Source
Food Recall
External ID
H-0155-2026
Action Date
2025-11-12
Status
Terminated
Category
food
Product Description
Giant/Martin's Crunchy Taco Dinner Kit, Net Wt 9.4 OZ (266g), UPC: 068826757516, DISTRIBUTED BY: ADUSA DISTRIBUTION, LLC SALISBURY, NC 28147 Product consists of 12 taco shells, 1 sauce packet, and 1 seasoning packet within a carton; packed 12 cartons per case
Lot/Code Info: Lot 25257, BEST IF USED BY MAR 13 26
Quantity Affected: 336 cases (4,032 units)
Reason for Recall
Undeclared allergen - milk
Distribution
AL, CT, FL, IN, MD, MI, NC, NY, OH, PA, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-10
Company
Louisville, KY
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 34 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Teasdale Foods, Inc. has 2 FDA actions in our database, including 2 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 (Teasdale Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Teasdale Foods, Inc. have FDA actions?
Teasdale Foods, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0155-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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