Recall record at a glance
| Official record | F-1564-2016 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | NatureBox, Inc. |
| Report date | Jun 29, 2016 |
| Recall initiation date | Jun 3, 2016 |
| Quantity | 22,231 x 5 oz. pouches. |
| Location | Redwood City, CA, United States |
Official product description
NatureBox Cheddar and Onion Sunflower kernels: 5 oz. (142g) customer stand up pouch. UPC: 8 54557 00531 1 Ingredients: Non GMO Sunflower kernels, Sunflower Oil, Sweet Onion and White Cheddar Seasoning Blend (cane sugar, onion and garlic powder, cheddar cheese powder {cheddar cheese (pasteurized milk, cheese cultures, salt, enzymes), buttermilk, whey, salt, disodium phosphate}, salt, natural flavors, lactic acid, spices, silicon dioxide (to prevent caking). Contains: Milk. Distributed by NatureBox, San Carlos, CA 94070
Why the product was recalled
Firm was notified by supplier of sunflower seeds that they are being recalled due to Listeria Monocytogenes.
Distribution information
Nationwide directly to consumers through online purchase.
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: E-Mail.
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.