Class IIOngoingVoluntary: Firm initiated
QUESO PALMITA GP LLC: food recall H-0015-2027
QUESO PALMITA GP LLC of Stafford, TX recalled QUESO PALMITA. Generic Name: Pastel de Queso (Cheese Pie). Intended use: Human consumption. Condition: Frozen. Shelf… Reason: Undeclared milk, cheese declared. The FDA listed it as Class II in its Enforcement Report dated Oct 14, 2026; distribution: Texas.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- QUESO PALMITA. Generic Name: Pastel de Queso (Cheese Pie). Intended use: Human consumption. Condition: Frozen. Shelf life or expected life: 90 days. Type of packaging: Vacuum, resealable package. Net weight: 1.2 lbs. UPC: 094922980045.
- Product quantity
- 20 packages
- Reason for recall
- Undeclared milk, cheese declared
- Codes, lots and dates on the package
- Manufacturing code: PQ02. Batch/lot code: PQ-1-0024. Manufacturing date: 04/22/2026. Packing date: 04/22/2026. Best By: 10/22/2026. Expiration date: 10/22/2026.
- Distribution pattern
- Texas
- Recalling firm
- QUESO PALMITA GP LLC, Stafford, TX
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Telephone
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Sep 15, 2026 |
| Classified by the FDA | Oct 7, 2026 |
| Published in the Enforcement Report | Oct 14, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0015-2027 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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