PEANUT BUTTER CHOCOLATE FUDGE BAR - 8 oz.
Recalling firm: Fudgeamentals LLC
Why it was recalled
made with peanut butter contaminated with Salmonella
The exact product
PEANUT BUTTER CHOCOLATE FUDGE BAR - 8 oz.
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
GTIN: 10840235800023 UPC: 840235800026 LOT: 22042001, 22059010, 22083003, 22089003, 22129378, 22059004
| Type | Code / value | Context |
|---|---|---|
| UPC | 840235800026 | GTIN: 10840235800023 UPC: 840235800026 LOT: 22042001, 22059010, 22083003, 22089003, 22129378, 22059004 |
| lot | 22042001 | GTIN: 10840235800023 UPC: 840235800026 LOT: 22042001, 22059010, 22083003, 22089003, 22129378, 22059004 |
| lot | 22059004 | 800023 UPC: 840235800026 LOT: 22042001, 22059010, 22083003, 22089003, 22129378, 22059004 |
| lot | 22059010 | GTIN: 10840235800023 UPC: 840235800026 LOT: 22042001, 22059010, 22083003, 22089003, 22129378, 22059004 |
| lot | 22083003 | GTIN: 10840235800023 UPC: 840235800026 LOT: 22042001, 22059010, 22083003, 22089003, 22129378, 22059004 |
| lot | 22089003 | GTIN: 10840235800023 UPC: 840235800026 LOT: 22042001, 22059010, 22083003, 22089003, 22129378, 22059004 |
| lot | 22129378 | : 10840235800023 UPC: 840235800026 LOT: 22042001, 22059010, 22083003, 22089003, 22129378, 22059004 |
Recall details
- Recall number
- F-1365-2022
- Event ID
- 90282
- FDA status
- Terminated
- Initiated
- May 24, 2022
- Reported
- Jul 6, 2022
- Classified
- Jun 24, 2022
- Terminated
- Oct 27, 2022
- Quantity
- 189,096 saleable units total
- 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-1365-2022
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.