FDA recall record

Hampton Creek Foods JUST Devil's Food Cake Mix recall — FDA F-2019-2016

Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.

Class Iclassification
F-2019-2016official record ID
Sep 7, 2016report date

Recall record at a glance

Official recordF-2019-2016
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmHampton Creek Foods
Report dateSep 7, 2016
Recall initiation dateJul 29, 2016
Quantity3,786 cases (6 units per cse)
LocationSan Francisco, CA, United States

Official product description

JUST Devil's Food Cake Mix; NET WT 20 oz. (1 lb 4 oz) 567 g); UPC 8 54829 00643 5. Ingredients: Muffin Mix: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour, niacin, reduced Iron, thiamine Monocitrate, riboflavin, folic acid), Sugar, Palm Oil., Alkalized Cocoa. . Contains less than 2% of Baking Powder )Sodium acid pyrophosphate, sodium bicarbonate, corn starch, monocalcium phosphate) Baking Soda, Citric Acid, Coconut Milk Powder (coconut milk, tapioca syrup), Natural Flavors, Oat Bran, Oat Hull Fiber, Salt, Sodium Aliginate, Sorghum Flour, Soy milk powder, Xanthan Gum. Blueberry Mix: Blueberries, Water: Crumble Mix: Sugar, Brown Sugar, Maltodextrin, Palm Oil, Enriched flour (wheat flour, malted barley flour, niacin, reduced iron, thiamine monocitrate, riboflavin, folic acid), cinnamon, Salt, Natural Flavors: Contains: Wheat, Soy, Coconut. Bake at 350 degrees for 24-34 minutes depending on pan size. Distributed by Hampton Creek, Inc., San Francisco, CA 94103.

Why the product was recalled

Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.

Distribution information

Nationwide to Wal-Mart stores

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

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.