Cardona Foods, Inc. Recall: Undeclared allergen milk (whey) and undeclared lard
United States
TerminatedClass II
- Company
- Cardona Foods, Inc.
- Product
- Uncooked Tortillas: FTC010 - Flour Tortilla 6 Taco Casa-…
- Recall date
- February 12, 2024
- Terminated
- March 18, 2025
- Source
- FDA
Reason for recall
Undeclared allergen milk (whey) and undeclared lard
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Uncooked Tortillas: FTC010 - Flour Tortilla 6 Taco Casa- 18/20 Count 18/22oz 18/624 grams FTC030 - Flour Tortilla 10 Taco Casa- 10/12 Count 10/32oz 10/907 grams | Not published in this source record | 9,302 cases | Manufactured 1/2/24 and 2/12/2024 |
Distribution
- Firm's customer is a restaurant chain located primarily in Texas. There is one location in Oklahoma.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1155-2024
- Event ID
- 94368
- Status
- Terminated
- Classification
- Class II
- Company
- Cardona Foods, Inc.
- Product description
- Uncooked Tortillas: FTC010 - Flour Tortilla 6 Taco Casa- 18/20 Count 18/22oz 18/624 grams FTC030 - Flour Tortilla 10 Taco Casa- 10/12 Count 10/32oz 10/907 grams
- Quantity
- 9,302 cases
- Reason
- Undeclared allergen milk (whey) and undeclared lard
- Recall initiation date
- February 12, 2024
- Report date
- April 24, 2024
- Classification date
- Not published in this source record
- Termination date
- March 18, 2025
- Distribution pattern
- Firm's customer is a restaurant chain located primarily in Texas. There is one location in Oklahoma.
- UPC, lot, and code information
- Manufactured 1/2/24 and 2/12/2024
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Cardona Foods, Inc.
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:
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.
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