Class IITerminated in FDA datasetJan 8, 2024

the original BENNY T'S VESTA DRY HOT SAUCE SCORPION NWT WT. 1.5OZ

Recalling firm: Benny Ts Vesta Inc dba Vesta Firey Gourmet Toppings

Why it was recalled

The firm was notified by the North Carolina Dept of Agriculture and Consumer Services that the product labeling does not include wheat and other ingredient common names in the ingredient statement.

Check your package

Compare the exact product and package details with the label you have.

Productthe original BENNY T'S VESTA DRY HOT SAUCE SCORPION NWT WT. 1.5OZ INGREDIENTS: Fresh Chilies, Onions, Breadcrumbs (enriched flour, water, sugar, yeast, salt, non-hydrogenated vegetable shortening), Olive Oil, Salt, Natural Preservatives. UPC 7 94571 99491 1 (Trinidad Moruga Scorpion)
UPC794571994911

FDA code information

LOT # 37 9/24

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

the original BENNY T'S VESTA DRY HOT SAUCE SCORPION NWT WT. 1.5OZ INGREDIENTS: Fresh Chilies, Onions, Breadcrumbs (enriched flour, water, sugar, yeast, salt, non-hydrogenated vegetable shortening), Olive Oil, Salt, Natural Preservatives. UPC 7 94571 99491 1 (Trinidad Moruga Scorpion)

Extracted codes and context

TypeCode / valueContext
UPC794571994911ydrogenated vegetable shortening), Olive Oil, Salt, Natural Preservatives. UPC 7 94571 99491 1 (Trinidad Moruga Scorpion)

Recall details

Recall number
F-0800-2024
Event ID
93756
FDA status
Terminated
Initiated
Jan 8, 2024
Reported
Feb 7, 2024
Classified
Jan 26, 2024
Terminated
Dec 17, 2025
Quantity
15/1.5 oz jars
Location
Raleigh, NC, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

Product was shipped to the following states: AL, AZ, CA, CO, CT, FL, GA, IL, KY, MD, MI, MN, MO, NC, NJ, NY, OH, OK, OR, PA, SC, TN, TX & VA.

FDA source record · F-0800-2024

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.