Recall record at a glance
| Official record | F-0735-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | B&G Foods North America, Inc. |
| Report date | Dec 24, 2014 |
| Recall initiation date | Nov 14, 2014 |
| Quantity | 7,201,809 cases total |
| Location | Parsippany, NJ, United States |
Official product description
Taco Seasoning Packets sold under the following brands, container size, and or as part of a dinner Kit: 1. Ortega 1.25 oz, UPC 39000-00820; 2. Ortega 3-pack, 3.75 oz. UPC 39000-00821; 3. Ortega Foodservice 5 lb. UPC 39000-00860 and 9 oz. 39000-00861; 4. Las Palmas 3-pack 3.75 oz. UPC 41501-79811 and (Canada) 106 g. UPC 41501-79812; 5. Ortega Taco Dinner Kit 10 oz., UPC 39000-00805; 6. Ortega Taco Dinner Kit 16.7 oz., UPC 39000-00818; 7. Ortega Soft Taco Dinner Kit 15.2 oz., UPC 39000-01012; 8. Ortega Whole Grain Taco Kit 9.15 oz., UPC 41501-00806; 9. Ortega "Tacos for Two" Kit 5 oz., UPC 41501-00832 and (Canada) 144 g. UPC 41501-00882; 10. Ortega Whole Wheat Soft Taco Kit 13.6 oz., UPC 41501-01014; 11. Ortega Grande Hard & Soft Taco Dinner Kit 15.9 oz., UPC 41501-01015; 12. Ortega Whole Grain/Whole Wheat Hard & Soft Taco Kit 15.9 oz., UPC 41501-01058; 13. Ortega Fiesta Flats Kit 9.8 oz., UPC 41501-08351;
Why the product was recalled
Specific Ortega Brand Taco Seasoning, Taco Sauce, Taco Dinner Kits, and Enchilada Sauce, and Las Palmas brand Taco Seasoning and Taco Sauce products are being recalled because one or more of the spice ingredients may contain peanuts and almonds.
Distribution information
Nationwide and Worldwide to include: Bermuda, Canada, Dominican Republic, Dubai, Guam, Haiti, Honduras, Israel, New Zealand, Panama, Philippines, Singapore, Trinidad, United Kingdom.
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
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.