FDA recall record

Spagel Brothers Stanganellis Italian Foods, Pumpkin Cake Roll, Net Wt recall — FDA F-1324-2019

Stanganellis Italian Foods, is initiating a recall of Pumpkin Cake Roll, Net Wt. 24 oz. . One per package, because of product miss-labeling. The firm…

Class IIclassification
F-1324-2019official record ID
May 8, 2019report date

Recall record at a glance

Official recordF-1324-2019
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSpagel Brothers, Inc.
Report dateMay 8, 2019
Recall initiation dateMar 26, 2019
Quantity80 Rolls
LocationErie, PA, United States

Official product description

Stanganellis Italian Foods, Pumpkin Cake Roll, Net Wt. 24 oz. . One pie per package . Box.

Why the product was recalled

Stanganellis Italian Foods, is initiating a recall of Pumpkin Cake Roll, Net Wt. 24 oz. . One per package, because of product miss-labeling. The firm inadvertently left off the allergen statement that soy was used in making the product.

Distribution information

Distributed in PA

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: E-Mail.

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.