Nutiva O'Coconut Lightly Sweetened Coconut Treat - Classic Sold in 8 - x 0.5 oz. individually wrapped pieces, UPC 6-92752-10557-9 and Si...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (laceration). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1920-2015.
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.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1920-2015.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Nutiva or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1920-2015.
Nutiva
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Nutiva Recall FAQ
Nutiva is the subject of a food safety report: Nutiva O'Coconut Lightly Sweetened Coconut Treat - Classic Sold in 8 - x 0.5 oz. individually wrapped pieces, UPC 6-92752-10557-9 and Si.... The notice was published on March 21, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 15,000 units are potentially affected.