Recall record at a glance
| Official record | F-1921-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Nutiva |
| Report date | Apr 15, 2015 |
| Recall initiation date | Mar 21, 2015 |
| Quantity | 8286 retail units |
| Location | Richmond, CA, United States |
Official product description
Nutiva O'Coconut Lightly Sweetened Coconut Treat - Hemp & Chia. Sold in Singles of 24 - 0.5 oz, per box - 6-92752-10502-9 24 singles x 6 caddies per shipping case - 144 individual units per case. Certified Organic, Fair Trade Certified. Manufactured for: Nutiva, 213 W. Cutting Blvd, Richmond, CA 94904.
Why the product was recalled
Contract manufacturer notified Nutiva that a positive lab result for Salmonella was found in desiccated coconut flakes used to manufacture a confectionery coconut bar product . This issue was initially identified during the daily lab testing of the finished product.
Distribution information
Nationwide through internet sales and three distribution sites in CA, TX.
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: Press Release.
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.