FDA recall record

Tarts A La Carte, LLC dba Blazo Pie shoppe 9-inch pie Blazos Pie Shoppe Chocolate Peanut recall — FDA F-1500-2022

Blazos Pie Shoppe Peanut Butter Cream Pie, Chocolate Peanut Butter Cream Pie and Peanut Butter Cream Cup products possibly contaminated with Salmonella.

Class Iclassification
F-1500-2022official record ID
Jul 27, 2022report date

Recall record at a glance

Official recordF-1500-2022
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmTarts A La Carte, LLC dba Blazo Pie shoppe LLC
Report dateJul 27, 2022
Recall initiation dateJun 21, 2022
Quantity3 units
LocationLivonia, MI, United States

Official product description

9-inch pie Blazos Pie Shoppe Chocolate Peanut Butter Cream Pie (UPC 9438600049) 9-inch pie Blazos Pie Shoppe Peanut Butter Cream Pie (UPC 9438600025)

Why the product was recalled

Blazos Pie Shoppe Peanut Butter Cream Pie, Chocolate Peanut Butter Cream Pie and Peanut Butter Cream Cup products possibly contaminated with Salmonella.

Distribution information

MI

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

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

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.