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CriticalFDAfda-F-1840-2016UNDECLARED ALLERGEN

7-ELEVEN FRESH TO GO CHOCOLATE CHUNK COOKIE NET WT. 4.0 OZ UPC: 052548558741

⚠ 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.

Units Affected
22,346
Recall Date
April 23, 2016
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1840-2016.

Undeclared peanuts

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1840-2016.

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 Bakery Express Of Southern California 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-1840-2016.

Bakery Express of Southern California

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.

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📣 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

Bakery Express Of Southern California Recall FAQ

Bakery Express Of Southern California is the subject of a bakery & grains safety report: 7-ELEVEN FRESH TO GO CHOCOLATE CHUNK COOKIE NET WT. 4.0 OZ UPC: 052548558741. The notice was published on April 23, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 22,346 units are potentially affected.