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CriticalFDAfda-F-1819-2014UNDECLARED ALLERGEN

Orton Bros. Brand Zesty Lemon Cookie Buttons; 6 oz. yellow box, UPC code 20104 19100. The lot code and expiration date are stamped on th...

⚠ 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
1,188
Recall Date
March 24, 2014
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1819-2014.

Undeclared peanuts.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1819-2014.

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 Vermont Common Foods, Llc 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-1819-2014.

Vermont Common Foods, LLC

FDA

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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.

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Vermont Common Foods, Llc Recall FAQ

Vermont Common Foods, Llc is the subject of a bakery & grains safety report: Orton Bros. Brand Zesty Lemon Cookie Buttons; 6 oz. yellow box, UPC code 20104 19100. The lot code and expiration date are stamped on th.... The notice was published on March 24, 2014 by the U.S. Food and Drug Administration (FDA). Approximately 1,188 units are potentially affected.