FDA recall record

Dough-To-Go Zoe's Cookies Vegan Tuxedo Fudge, 4 oz recall — FDA F-1537-2018

Undeclared allergen; walnuts

Class Iclassification
F-1537-2018official record ID
Jun 13, 2018report date

Recall record at a glance

Official recordF-1537-2018
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmDough-To-Go Inc.
Report dateJun 13, 2018
Recall initiation dateMay 24, 2018
Quantity20 cases (24 x 4 oz. cookies per case)
LocationSanta Clara, CA, United States

Official product description

Zoe's Cookies Vegan Tuxedo Fudge, 4 oz. (153 kg) individually wrapped cookie. INGREDIENTS: UNBLEACHED FLOUR (WHEAT FLOUR, NIACIN, IRON, THIAMINE MONONITRATE, RIBOFLAVIN, ENZYME, FOLIC ACID), EVAPORATED CANE JUICE, VEGAN WHITE CHOCOLATE CHIPS (NON-BONE CHAR PROCESSED SUGAR, VEGETABLE OIL, COCOA BUTTER, SOY LECITHIN, VANILLIN, SALT, VEGAN NATURAL FLAVORS), BANANA PUREE, NATURAL BUTTERY SPREAD (NATURAL OIL BLEND OF PALM FRUIT, CANOLA, AND OLIVE OILS, FILTERED WATER, PURE SALT, NATURAL FLAVOR, SUNFLOWER LECITHIN, NON DAIRY LACTIC ACID, ANNATTO EXTRACT), COCOA POWDER, DARK COCOA POWDER, BAKING SODA, VANILLA, CHOCOLATE EXTRACT, SALT. (MANUFACTURED ON SHARED EQUIPMENT WITH EGGS, DAIRY, TREE NUTS, AND PEANUTS.) CONTAINS: WHEAT, SOY. UPC 0 44964-13340 4 Product of Dough-To-GO Inc.

Why the product was recalled

Undeclared allergen; walnuts

Distribution information

U.S. distribution to the following: CA. No foreign 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: Telephone.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.