Casa Mamita Soft Taco Dinner Kit
Reason Undeclared allergen - milk
Giant/Martin's Crunchy Taco Dinner Kit recall
Recalled by Teasdale Foods, Inc. · Louisville, KY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Undeclared allergen - milk
Undeclared allergen: Milk
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
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
Quantity: 336 cases (4,032 units)
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot 25257, BEST IF USED BY MAR 13 26
Where it was sold
Alabama Connecticut Florida Indiana Maryland Michigan North Carolina New York Ohio Pennsylvania Wisconsin
FDA's distribution note: AL, CT, FL, IN, MD, MI, NC, NY, OH, PA, WI
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Teasdale Foods, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 10, 2025
- In FDA report of
- Nov 12, 2025
- Terminated
- Apr 29, 2026
- FDA recall number
- H-0155-2026 · event 97813
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.