Food recall: Nutiva O'Coconut Lightly Sweetened Coconut Treat - Classic Sold in 8 - x 0.5 oz. individually wrapped pieces, UPC…
Class I FDA enforcement event 70801. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
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.
Class I, in the words of FDA
a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death
Nutiva started this food recall on 21 Mar 2015. The firm address in the FDA record is in Richmond, CA. FDA put the recall in Class I. FDA event 70801 has 2 product records. The first FDA enforcement report date is 15 Apr 2015. The record gives the status Terminated, with the termination date 8 Jun 2015.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
Nationwide through internet sales and three distribution sites in CA, TX.
Recalling firm
Nutiva, Richmond, CA.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
2 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1920-2015 | Nutiva O'Coconut Lightly Sweetened Coconut Treat - Classic Sold in 8 - x 0.5 oz. individually wrapped pieces, UPC 6-92752-10557-9 and Singles of 24 - 0.5 oz, per box - UPC 6-92752-10500-5. - 24 singles x 6 caddies per shipping case - 144 individual units. Certified Organic, Fair Trade Certified. Manufactured for:… | 15,000 retail units bar 312, 2,400 retail units bar 302. | Class I | Terminated | 15 Apr 2015 |
| F-1921-2015 | 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. | 8286 retail units | Class I | Terminated | 15 Apr 2015 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class I: The highest of the three FDA recall classes.
The event in context
- Food events that started in 2015
- 607
- Share of these events in Class I
- 47%
- Product records in this event
- 2Median of the firm: 2
- Events of the firm on the register
- 2
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 17 Mar 2017 | Nutiva Nuture Vitality Organic Plant Protein Superfood 30 Shake - Vanilla; Product # PBP201 - 10-1.2 oz. packets; Packet | Food | Class I | 2 |
Official channels
- FDA enforcement report F-1920-2015The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
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Cite this page
Recall Register. FDA enforcement event 70801. https://recallregister.com/fda/i/70801/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
Nationwide through internet sales and three distribution sites in CA, TX.
- What quantity of product is in FDA event 70801?
- The event has 2 product records. The first record gives this quantity:
15,000 retail units bar 312, 2,400 retail units bar 302.
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2015 have the same class?
- 47% of the 607 food events that started in 2015 are in Class I.