Recall record at a glance
| Official record | F-1091-2024 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Reser's Fine Foods, Inc. |
| Report date | Mar 27, 2024 |
| Recall initiation date | Feb 6, 2024 |
| Quantity | Item 404764 DP Express Meal Kit = 1236 kits; Other Taco Kits = 24,582 kits |
| Location | Beaverton, OR, United States |
Official product description
Item 404764, KIT EM CHICKEN STREET TACO DP EXPRESS MEAL 6/22 OZ, UPC 7111712500. The following Taco Kits were distributed to consignees with instructions for assembly at retail store kitchen: Item 406987, KIT OP CHICKEN TACO MINI SINGLE SERVE ON PREMISE NO TRAYS 2/2.4925 LB, UPC 1345438444. Item 407012, KIT OP CHICKEN TACO MINI SINGLE SERVE ON PREMISE WITH TRAYS 2/2.4925 LB, UPC 1345438460. Item 404894, KIT OP CHICKEN TACO SINGLE SERVE ON PREMISE NO TRAYS 1/4.9875 LB, UPC 1345438162. Item 404700 KIT OP PREMIUM CHICKEN STREET TACO ON PREMISE WITH TRAYS 2/4.9875 LB, UPC 1345438075. Item 404711, KIT OP STREET TACO CHICKEN ON PREMISE NO TRAY DP 2/4.985 LB, UPC 1345438082. Item 404710, KIT OP STREET TACO CHICKEN ON PREMISE WITH TRAY DP 2/4.985 LB, UPC 1345438080. Item 406581, KIT OP STREET TACO CHICKEN ON PREMISE WITH TRAY HOME CHEF 2/4.985 LB, UPC 4013430435.
Why the product was recalled
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
Distribution information
Distributed in CA, CT, FL, ID, IL, MD, MT, NJ, NV, OR, PA, SD, TX, UT, VA, and WA.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
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