FDA recall record

The James Skinner Co Marketside Cinnamon Pecan Braid, Triple-Filled Danish, Filled recall — FDA F-1417-2024

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

Class IIclassification
F-1417-2024official record ID
Jul 3, 2024report date

Recall record at a glance

Official recordF-1417-2024
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmThe James Skinner Co.
Report dateJul 3, 2024
Recall initiation dateApr 11, 2024
Quantity4111 cases / 24666 packages
LocationOmaha, NE, United States

Official 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.

Why the product was recalled

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

Distribution information

Nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Other.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.