Class ITerminated in FDA datasetRecall initiated May 24, 2022

Fudgeamentals TIGER BUTTER FUDGE BAR (8 OZ)

Recalling firm: Fudgeamentals LLC

Why it was recalled

made with peanut butter contaminated with Salmonella

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 27, 2022.

Check your package

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

ProductFudgeamentals TIGER BUTTER FUDGE BAR (8 OZ)
Package size8 OZ
UPC840235800811

FDA code information

GTIN: 10840235800818 UPC: 840235800811 LOT: 22059007, 22083006, 22089006, 22130394

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

Full FDA record and distribution details

Original product description

Fudgeamentals TIGER BUTTER FUDGE BAR (8 OZ)

Extracted codes and context

TypeCode / valueContext
UPC840235800811GTIN: 10840235800818 UPC: 840235800811 LOT: 22059007, 22083006, 22089006, 22130394
lot22059007GTIN: 10840235800818 UPC: 840235800811 LOT: 22059007, 22083006, 22089006, 22130394
lot22083006GTIN: 10840235800818 UPC: 840235800811 LOT: 22059007, 22083006, 22089006, 22130394
lot22089006GTIN: 10840235800818 UPC: 840235800811 LOT: 22059007, 22083006, 22089006, 22130394
lot22130394GTIN: 10840235800818 UPC: 840235800811 LOT: 22059007, 22083006, 22089006, 22130394

Original FDA recall reason

made with peanut butter contaminated with Salmonella

Recall details

Recall number
F-1371-2022
Event ID
90282
FDA status
Terminated
Initiated
May 24, 2022
Reported
Jul 6, 2022
Classified
Jun 24, 2022
Terminated
Oct 27, 2022
Quantity
Not provided
Location
Melville, NY, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Nationwide

FDA source record · F-1371-2022

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

Follow official FDA and manufacturer guidance.