RecallHawk
Class II Recall

Publix Raspberry Coffee Cake, Net Wt. 15 oz. (425g), packaged in an aluminum foil tray and clear plastic clamshell lid w

The James Skinner LLC

Summary

The FDA issued a Class II for Publix Raspberry Coffee Cake, Net Wt. 15 oz. (425g), packaged in an aluminum foi by The James Skinner LLC. Reason: Undeclared allergen - walnuts. Maple Walnut Coffee Cake was incorrectly labeled as Raspberry Coffee Cake and walnuts were not declared on the label..

Details

Source

Food Recall

External ID

H-0330-2026

Action Date

2025-12-31

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: Product Lot Number: 5309 Expiration Date on Case: 5 1 04 FRZ EXP 110526

Quantity Affected: 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.

Distribution

Product shipped to one distributor in FL: Sourcing and Distribution Specialist Winter Haven, FL 33880

Type: Voluntary: Firm initiated

Recall Initiated: 2025-12-10

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (The James Skinner LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does The James Skinner LLC have FDA actions?

This is the only FDA action we have on record for The James Skinner LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0330-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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