Skip to main content
CriticalFDAfda-F-1531-2020UNDECLARED ALLERGEN

Frito-Lay 18 count Flavor Mix sack UPC 28400 15443 1 oz. individual bags packaged in a larger flexible bag

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
3,509
Recall Date
August 24, 2020
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1531-2020.

May contain undeclared milk

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1531-2020.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Frito-lay, Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1531-2020.

Frito-Lay, Inc.

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

Visit FDA.gov →

📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

How to report to FDAFile a report at FDA

Frito-lay, Inc. Recall FAQ

Frito-lay, Inc. is the subject of a food safety report: Frito-Lay 18 count Flavor Mix sack UPC 28400 15443 1 oz. individual bags packaged in a larger flexible bag. The notice was published on August 24, 2020 by the U.S. Food and Drug Administration (FDA). Approximately 3,509 units are potentially affected.