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CriticalFDAfda-F-0006-2021UNDECLARED ALLERGEN

Goodie Girl, Gluten Free Magical Animal Crackers, 7 ounce , paper cartons, 6 packages per case, Best By JAN 11 21 A3

⚠ 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
385
Recall Date
September 4, 2020
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0006-2021.

Gluten free product was mixed with wheat containing product. Undeclared Wheat.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0006-2021.

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 Toufayan Bakery, 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-0006-2021.

Toufayan Bakery, Inc.

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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Toufayan Bakery, Inc. Recall FAQ

Toufayan Bakery, Inc. is the subject of a bakery & grains safety report: Goodie Girl, Gluten Free Magical Animal Crackers, 7 ounce , paper cartons, 6 packages per case, Best By JAN 11 21 A3. The notice was published on September 4, 2020 by the U.S. Food and Drug Administration (FDA). Approximately 385 units are potentially affected.