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The James Skinner Co. Recall: Product has incorrect back label that does not declare pecans are present in the product.

United States

TerminatedClass II

Company
The James Skinner Co.
Product
Marketside Cinnamon Pecan Braid, Triple-Filled Danish, Fille…
Recall date
April 11, 2024
Terminated
September 15, 2025
Source
FDA

Reason for recall

Product has incorrect back label that does not declare pecans are present in the product.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Marketside Cinnamon Pecan Braid, Triple-Filled Danish, Filled with Cinnamon Filling, Topped with Pecans, Sweet Icing and Streusel. Net Wt. 18 oz (1 lb 2 oz) 510g. UPC 7874202922. 6 units per case. 7874202922 4111 cases / 24666 packages Package Lot 4 073 2; Expiration date on case: FRZ EXP 031325

Distribution

  • Nationwide

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1417-2024
Event ID
94402
Status
Terminated
Classification
Class II
Company
The James Skinner Co.
Product description
Marketside Cinnamon Pecan Braid, Triple-Filled Danish, Filled with Cinnamon Filling, Topped with Pecans, Sweet Icing and Streusel. Net Wt. 18 oz (1 lb 2 oz) 510g. UPC 7874202922. 6 units per case.
Quantity
4111 cases / 24666 packages
Reason
Product has incorrect back label that does not declare pecans are present in the product.
Recall initiation date
April 11, 2024
Report date
July 3, 2024
Classification date
Not published in this source record
Termination date
September 15, 2025
Distribution pattern
Nationwide
UPC, lot, and code information
UPC 7874202922; Package Lot 4 073 2; Expiration date on case: FRZ EXP 031325
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Other
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: The James Skinner Co.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.