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CriticalFDAfda-F-1878-2013UNDECLARED ALLERGEN

First Street Coffee Cake Muffins (S 45398) 4 count 14 oz. UPC 0 4151210848 8

⚠ 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
8,478
Recall Date
August 26, 2013
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1878-2013.

Bubbles Baking Co. is recalling coffee cake muffins because it may contain undeclared pecan nuts.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1878-2013.

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 Kdk Management, Inc., Dba Bubbles Baking Co. 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-1878-2013.

KDK Management, Inc., dba Bubbles Baking Co.

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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Kdk Management, Inc., Dba Bubbles Baking Co. Recall FAQ

Kdk Management, Inc., Dba Bubbles Baking Co. is the subject of a bakery & grains safety report: First Street Coffee Cake Muffins (S 45398) 4 count 14 oz. UPC 0 4151210848 8. The notice was published on August 26, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 8,478 units are potentially affected.