FDA recall record

Biscomerica Sweet Serenity Caramel Sea Salt Chocolate Chip Cookies, with recall — FDA F-1680-2018

Product labeling does not list milk in the contains statement; however milk is listed as in ingredient.

Class IIclassification
F-1680-2018official record ID
Aug 1, 2018report date

Recall record at a glance

Official recordF-1680-2018
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBiscomerica, Inc.
Report dateAug 1, 2018
Recall initiation dateJul 20, 2018
Quantity14,716 cs
LocationRialto, CA, United States

Official product description

Sweet Serenity Caramel Sea Salt Chocolate Chip Cookies, with caramel flavored chips; NET WT; 2 oz. UPC: 0 31535 59962 2 Manufactured by Biscomerica Corp, Rialto, CA Ingredients: Enriched unbleached flour (wheat flour, niacin, reduced iron, thiamine mononitrate {Vitamin B1}, Riboflavin {Vitamin B2} Folic acid), palmsoy margarine (palm oil, soybean oil, water, contains less than 2% salt, vegetable mono & diglycerides, soy lecithin, sodium benzoate (a preservative), citric acid, natural and artificial flavor, Vitamin A, Palmitate added, Beta Carotene (color) Caramel chips (Sugar, vegetable fat (palm kernel and or palm) nonfat dry milk color added, soy lecithin (an emulsifier) natural flavors, paprika oleoresin color, semi-sweet chocolate chips (sugar, unsweetened chocolate, cocoa butter, sol lecithin (an emulsifier) vanilla, brown sugar, sugar, water, sea salt, dried eggs, baking soda, salt , soy lecithin, natural and artificial flavor, ammonium bicarbonate. Allergy information - contains Wheat, egg and soy ingredients. May contain milk and tree nuts.

Why the product was recalled

Product labeling does not list milk in the contains statement; however milk is listed as in ingredient.

Distribution information

CT, NJ, GA, FL, TN, TX, IL, OH, MI, MO, CA, CO, MN, NC, TX, NY, VA, OR, AZ, WI, AL, MD, NY, LA.

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: Letter.

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.