Sweet Serenity Caramel Sea Salt Chocolate Chip Cookies, with caramel flavore...
FDA Recall #F-1680-2018 — Class II — July 20, 2018
Recall Summary
| Recall Number | F-1680-2018 |
| Date Initiated | July 20, 2018 |
| Classification | Class II |
| Status | Terminated |
| Type | Voluntary: Firm initiated |
| Product Type | Food |
Recalling Firm
| Firm | Biscomerica, Inc. |
| Location | Rialto, CA |
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.
Reason for Recall
Product labeling does not list milk in the contains statement; however milk is listed as in ingredient.
Classification
Class II — A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution Pattern
CT, NJ, GA, FL, TN, TX, IL, OH, MI, MO, CA, CO, MN, NC, TX, NY, VA, OR, AZ, WI, AL, MD, NY, LA.
Product Quantity
14,716 cs
Product Codes / Lot Numbers
Code dates with expiration date of AB052918, AB071818, AB072518, AB072818, AB082818, AB100518, AB111618, BB052918, BB090818, BB011119, BB021819, CB052918, CB071718, CB080318, CB082718, CB100418, CB111518, CB011119
What Should You Do?
Stop consuming this product immediately. Check your home for the recalled item and dispose of it safely. If you experienced a health issue after consuming this product, contact your doctor and report it to the FDA MedWatch.
Frequently Asked Questions
Stop consuming the product immediately and do not donate or give it to others. Check the recall notice above for specific disposal or return instructions. Many food recalls ask you to throw the product away and retain the packaging for a possible refund from the retailer. If you purchased it online, check your order history — some retailers send recall notifications directly to customers. You do not need a receipt to report an issue or seek a refund; the fact of purchase is typically sufficient.
In most cases, yes. Retailers are typically notified to accept returns of recalled products and issue refunds, regardless of whether you have a receipt. Check with the store where you purchased the item. Some manufacturers also offer direct refunds — contact the recalling firm using the information in the official recall notice. If you purchased the product online, contact the retailer's customer service with your order number. In either case, you generally do not need original packaging, though retaining the product label with the lot code or UPC can speed up the process.
Report foodborne illnesses and adverse food reactions to the FDA through the MedWatch Safety Reporting Portal at FDA.gov, or by calling 1-800-332-1088. You can also report issues directly to the FDA's Safety Reporting Portal at SafetyReporting.hhs.gov. If you believe there is an immediate public health risk, contact your local health department. Your report helps the FDA identify contamination patterns, initiate recalls faster, and protect other consumers from the same hazard. Include as much detail as possible: the product name, lot code, purchase date and location, and a description of your symptoms or findings.
The FDA assigns a status to each recall action throughout its lifecycle. "Ongoing" means the recall is active — the firm is still working to remove the product from commerce and notify consumers. "Completed" means the recall strategy has been implemented and the FDA has determined that the recalling firm has taken all appropriate steps to remove the product. "Terminated" means the FDA has reviewed the results and concluded the recall is complete. Even if a recall is marked as completed or terminated, you should still discard any recalled products you find at home — the recall status refers to the firm's compliance actions, not the safety of product still in consumers' possession.