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CriticalFDAfda-F-0866-2022UNDECLARED ALLERGEN

14" Raw Buttermilk Breakfast Tart with Fresh Blueberries & Granola P2006 (9 Frozen Pancakes). Barcode:0106915030162006992202425990

⚠ 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
59
Recall Date
February 23, 2022
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0866-2022.

Undeclared almonds

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0866-2022.

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 Gourmet Kitchen, 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-0866-2022.

Gourmet Kitchen, 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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Gourmet Kitchen, Inc. Recall FAQ

Gourmet Kitchen, Inc. is the subject of a dairy safety report: 14" Raw Buttermilk Breakfast Tart with Fresh Blueberries & Granola P2006 (9 Frozen Pancakes). Barcode:0106915030162006992202425990. The notice was published on February 23, 2022 by the U.S. Food and Drug Administration (FDA). Approximately 59 units are potentially affected.