FDA recall record

NuGo Nutrition HQ 5g net carbs, A gluten-free, soy protein bar with overall recall — FDA F-2094-2017

Undeclared milk allergen. Brownie Bar packaged in Crunchy Peanut Butter Bar wrapper which does not list milk as an allergen under allergen information…

Class Iclassification
F-2094-2017official record ID
Apr 26, 2017report date

Recall record at a glance

Official recordF-2094-2017
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmNuGo Nutrition HQ
Report dateApr 26, 2017
Recall initiation dateMar 28, 2016
Quantity1165 cases
LocationOakmont, PA, United States

Official product description

NuGo Slim Crunchy Peanut Butter Protein Bar, 5g net carbs, A gluten-free, soy protein bar with overall peanut butter and chocolate taste covered in dark chocolate, Best Buy 07/28/2017, manufactured for: NuGo Nutrition 520 second Street, Oakmont, PA 15139 INGREDIENTS: SLIM PROTEIN [NON-GMO SOY CRISP (NON-GMO SOY PROTEIN, TAPIOCA, CALCIUM CARBONATE), NON-GMO SOY PROTEIN, NON-GMO RICE PROTEIN], BITTERSWEET DARK CHOCOLATE (CHOCOLATE LIQUOR, CANE SUGAR, COCOA BUTTER, VANILLA), CHICORY ROOT, VEGETABLE GLYCERINE, PEANUTS, CHOCOLATE LIQUOR, PEANUT FLOUR, ALMONDS, PEANUT EXTRACT, RICE BRAN, NATURAL FLAVORS, MICROCRYSTALLINE CELLULOSE, AND SALT. ALLERGEN INFORMATION: CONTAINS PEANUTS, ALMONDS AND SOY. MANUFACTURED ON EQUIPMENT THAT ALSO PROCESSES PRODUCTS CONTAINING TREE NUTS, MILK AND EGG. PRODUCT IS CERTIFIED PAREVE.

Why the product was recalled

Undeclared milk allergen. Brownie Bar packaged in Crunchy Peanut Butter Bar wrapper which does not list milk as an allergen under allergen information section of the ingredient statement.

Distribution information

Product was distributed throughout the United States. There were no international distribution.

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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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