FDA recall record

NatureBox Dark Cocoa Nom Noms 4.5oz recall — FDA F-0087-2017

Firm was notified by third party warehouse that some Peanut Butter Nom Nom product was packaged in Dark Cocoa Nom Nom packaging and therefore did not…

Class Iclassification
F-0087-2017official record ID
Oct 19, 2016report date

Recall record at a glance

Official recordF-0087-2017
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmNatureBox, Inc.
Report dateOct 19, 2016
Recall initiation dateMay 4, 2016
Quantity12,775 bags
LocationRedwood City, CA, United States

Official product description

Dark Cocoa Nom Noms 4.5oz. (128g) UPC: 8 54557 00533 5 Lot 16083 Product is shipped directly to customers per individual order or to corporate customers in 20 x 4.5 oz. bags cases. Ingredients: Rolled Oats, Almonds. For address freshness (Grape juice, rice dextrin), honey, sugar, canola oil, dark chocolate flavored chips (sugar, vegetable far {palm, palm kernel}, cocoa processed with alkali, dry buttermilk, soy lecithin (an emulsifier), natural flavors, Cocoa Powder, Egg Whites, Unsweetened Chocolate, unsweetened coconut, Brown Rice Syrup, natural flavor, pumpkin seeds, cocoa processed with alkali, salt. Contains: Tree nuts (almonds, coconut, Milk, Soy and Egg). Packed in a facility that also processes tree nuts, peanuts, milk, wheat, egg and soy. Distributed by Nature Box, San Carlos, CA

Why the product was recalled

Firm was notified by third party warehouse that some Peanut Butter Nom Nom product was packaged in Dark Cocoa Nom Nom packaging and therefore did not declare peanuts in the ingredient or allergen information.

Distribution information

Nationwide through direct purchase on web site.

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

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