Recall record at a glance
| Official record | F-2035-2016 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Hampton Creek Foods |
| Report date | Sep 7, 2016 |
| Recall initiation date | Jul 29, 2016 |
| Quantity | 3,731 (6 units per case) |
| Location | San Francisco, CA, United States |
Official product description
JUST Cinnamon Roll Coffee Cake Mix; NET WT 26.9 oz. (1 lb 10.9 oz) 762 g); UPC 8 54829 00644 2. Ingredients: Cake Mix: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour, niacin, reduced Iron, thiamine monomonitrate, riboflavin, folic acid), Sugar. Contains less than 2% of Baking Powder (sodium acid Pyrophosphate, sodium bicarbonate, corn starch, monocalcium phosphate), Baking Soda, Citric acid, Natural Flavors, Oat Bran, Oat Hull Fiber, Palm Oil, Salt, Sodium Aliginate, Sorghum Flour, Soy Milk Powder, X.an than Gum. Icing Mix: Powdered Sugar (dried cane syrup, corn starch), Canola Oil, Soy Milk Powder, Corn Starch, Modified Food Starch, Salt, Natural Flavors, Citric Acid. Swirl Mix: Brown Sugar, Sugar, Canola Oil, Invert Sugar, Cinnamon, Salt, Natural Flavors, Spice, Citric Acid. Yeast Pack: Yeast (yeast, Sorbitan monostearate, ascorbic acid. Contains: Wheat, Soy, Coconut. Bake at 350 degrees for 30-44 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.