FDA recall record

NatureBox 6 oz recall — FDA F-0756-2016

Third party warehouse discovered that they found bags of Cinnamon Yogurt Mini Graham products that were packaged in Probiotic Power Mix bags. Probiotic…

Class IIclassification
F-0756-2016official record ID
Mar 23, 2016report date

Recall record at a glance

Official recordF-0756-2016
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNatureBox, Inc.
Report dateMar 23, 2016
Recall initiation dateFeb 22, 2016
Quantity7419 x 6 oz. bags.
LocationRedwood City, CA, United States

Official product description

NatureBox Cinnamon Yogurt Mini Grahams, 6 oz. (170g) customer stand up pouches. UPC 8 58590 00528 4 Ingredients: Graham Crackers (unbleached unenriched wheat flour, whole wheat graham flour, sugar, palm and palm kernel oil, molasses, honey, salt, sodium bicarbonate). Yogurt Coating (sugar, palm kernel and/or palm oil, whey powder, Dry nonfat yogurt, soy lecithin (an emulsifier) salt, vanilla extract) Cinnamon. Contains:Wheat, Milk and Soy. Packed in a facility that also processes tree nuts, peanuts, milk, wheat, egg, soy and fish. Distributed by: Nature Box San Carlos, CA 94070

Why the product was recalled

Third party warehouse discovered that they found bags of Cinnamon Yogurt Mini Graham products that were packaged in Probiotic Power Mix bags. Probiotic bags do not properly declare wheat as an allergen.

Distribution information

Direct consumers through mail order.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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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