Marketside Cinnamon Pecan Braid
Reason Product has incorrect back label that does not declare pecans are present in the product.
Publix Raspberry Coffee Cake recall
Recalled by The James Skinner LLC · Omaha, NE, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Undeclared allergen - walnuts. Maple Walnut Coffee Cake was incorrectly labeled as Raspberry Coffee Cake and walnuts were not declared on the label.
Undeclared allergen: Tree nuts
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Publix Raspberry Coffee Cake, Net Wt. 15 oz. (425g), packaged in an aluminum foil tray and clear plastic clamshell lid with wraparound label, UPC 0-41415-54691-2, Distributed By Publix Supermarkets, Inc. Lakeland, FL 33802, packed 12 per case Case label reads, in part: Maple Walnut Coffee Cake, 12 units/14 oz. each, Net Wt. 10.5 LB (4.6 kg), UPC 100 41415 54591 2
Quantity: 811 cases
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Product Lot Number: 5309 Expiration Date on Case: 5 1 04 FRZ EXP 110526
Where it was sold
Florida
FDA's distribution note: Product shipped to one distributor in FL: Sourcing and Distribution Specialist Winter Haven, FL 33880
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to tree nuts; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- The James Skinner LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 10, 2025
- In FDA report of
- Dec 31, 2025
- Terminated
- Jan 15, 2026
- FDA recall number
- H-0330-2026 · event 98148
- Official record
- FDA enforcement report search
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