FRITO-LAY NORTH AMERICA, INC. Recall: Undeclared Allergen: Milk
United States
TerminatedClass I
- Company
- FRITO-LAY NORTH AMERICA, INC.
- Product
- Miss Vickies Spicy Dill Pickle; 8 oz bag
- Recall date
- March 3, 2026
- Terminated
- May 12, 2026
- Source
- FDA
Reason for recall
Undeclared Allergen: Milk
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Miss Vickies Spicy Dill Pickle; 8 oz bag | Not published in this source record | 5,292 bags | "Guaranteed Fresh" date of 21 APR 2026 And one of these 9-digit Manufacturing Codes 38U301414 48U101514 |
Distribution
- Arkansas
- Louisiana
- Mississippi
- New Mexico
- Oklahoma
- and Texas.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0571-2026
- Event ID
- 98538
- Status
- Terminated
- Classification
- Class I
- Company
- FRITO-LAY NORTH AMERICA, INC.
- Product description
- Miss Vickies Spicy Dill Pickle; 8 oz bag
- Quantity
- 5,292 bags
- Reason
- Undeclared Allergen: Milk
- Recall initiation date
- March 3, 2026
- Report date
- March 25, 2026
- Classification date
- Not published in this source record
- Termination date
- May 12, 2026
- Distribution pattern
- Arkansas, Louisiana, Mississippi, New Mexico, Oklahoma, and Texas.
- UPC, lot, and code information
- "Guaranteed Fresh" date of 21 APR 2026 And one of these 9-digit Manufacturing Codes 38U301414 48U101514
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Press Release
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: FRITO-LAY NORTH AMERICA, 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 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.
