10 oz Blazos Pie Shoppe Peanut Butter Cream Cup (UPC 9438600085)
Summary
The FDA issued a Class I for 10 oz Blazos Pie Shoppe Peanut Butter Cream Cup (UPC 9438600085) by Tarts A La Carte, LLC dba Blazo Pie shoppe LLC. Reason: Blazos Pie Shoppe Peanut Butter Cream Pie, Chocolate Peanut Butter Cream Pie and Peanut Butter Cream Cup products possibly contaminated with Salmonell.
Details
Source
Food Recall
External ID
F-1501-2022
Action Date
2022-07-27
Status
Terminated
Category
food
Product Description
10 oz Blazos Pie Shoppe Peanut Butter Cream Cup (UPC 9438600085)
Lot/Code Info: 6/23 and 6/27
Quantity Affected: 8 units
Reason for Recall
Blazos Pie Shoppe Peanut Butter Cream Pie, Chocolate Peanut Butter Cream Pie and Peanut Butter Cream Cup products possibly contaminated with Salmonella.
Distribution
MI
Type: Voluntary: Firm initiated
Recall Initiated: 2022-06-21
Company
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 88 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Tarts A La Carte, LLC dba Blazo Pie shoppe LLC has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Tarts A La Carte, LLC dba Blazo Pie shoppe LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Tarts A La Carte, LLC dba Blazo Pie shoppe LLC have FDA actions?
Tarts A La Carte, LLC dba Blazo Pie shoppe LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1501-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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