Frito-Lay 54 count Classic Mix cube box UPC 28400 30817, 1 oz. individual bag...
FDA Recall #F-1533-2020 — Class I — August 24, 2020
Recall Summary
| Recall Number | F-1533-2020 |
| Date Initiated | August 24, 2020 |
| Classification | Class I |
| Status | Terminated |
| Type | Voluntary: Firm initiated |
| Product Type | Food |
Recalling Firm
| Firm | Frito-Lay, Inc. |
| Location | Plano, TX |
Product Description
Frito-Lay 54 count Classic Mix cube box UPC 28400 30817, 1 oz. individual bags packaged in a larger box
Reason for Recall
May contain undeclared milk
Classification
Class I — A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Distribution Pattern
distributed in Arizona, California, Hawaii, Idaho, Montana, New Mexico, Nevada, Oregon, Utah, Washington and Wyoming to retail stores and via foodservice, vending, e-commerce, mail distribution and other channels.
Product Quantity
37632 bags
Product Codes / Lot Numbers
20OCT2020 6TC12210101; 20OCT2020 5TC12200101; 20OCT2020 4TC12190101; 20OCT2020 3TC12250101; 20OCT2020 3TC12180101; 20OCT2020 2TC12240101; 20OCT2020 2TC12230202; 03NOV2020 6TC12210101; 03NOV2020 5TC12270101; 03NOV2020 5TC12200101; 03NOV2020 4TC12260101; 03NOV2020 4TC12190101; 03NOV2020 3TC12320101; 03NOV2020 3TC12250101; 03NOV2020 3TC12180101; 03NOV2020 2TC12310101; 03NOV2020 2TC12240101; 03NOV2020 2TC12230202; 03NOV2020 1TC12300101; 03NOV2020 1TC12230101
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.
If you have a food allergy and consumed the recalled product, monitor yourself closely for allergic reaction symptoms — including hives, swelling, difficulty breathing, nausea, vomiting, or anaphylaxis. If you experience any symptoms, seek medical attention immediately. For anaphylaxis (severe allergic reaction with difficulty breathing, rapid heartbeat, or loss of consciousness), call 911 and use an epinephrine auto-injector (EpiPen) if available. Stop consuming the product and check all products from the same manufacturer for similar labeling issues, as undeclared allergens sometimes affect multiple products from the same production facility.
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.