Class IITerminatedVoluntary: Firm initiated
The James Skinner LLC: food recall H-0330-2026
The James Skinner LLC of Omaha, NE recalled Publix Raspberry Coffee Cake, Net Wt. 15 oz. (425g), packaged in an aluminum foil tray and clear plastic clamshell lid… Reason: Undeclared allergen - walnuts. Maple Walnut Coffee Cake was incorrectly labeled as Raspberry Coffee Cake and walnuts were not declared on the label. The FDA listed it as Class II in its Enforcement Report dated Dec 31, 2025; distribution: Florida.
Record status as published: Terminated (terminated Jan 15, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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
- Product quantity
- 811 cases
- Reason for recall
- Undeclared allergen - walnuts. Maple Walnut Coffee Cake was incorrectly labeled as Raspberry Coffee Cake and walnuts were not declared on the label.
- Codes, lots and dates on the package
- Product Lot Number: 5309 Expiration Date on Case: 5 1 04 FRZ EXP 110526
- Distribution pattern
- Product shipped to one distributor in FL: Sourcing and Distribution Specialist Winter Haven, FL 33880
- Recalling firm
- The James Skinner LLC, Omaha, NE
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Dec 10, 2025 |
| Classified by the FDA | Dec 19, 2025 |
| Published in the Enforcement Report | Dec 31, 2025 |
| Terminated | Jan 15, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0330-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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