Wholesale Produce Supply LLC DBA food recall: Cucumbers
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 96040
- Recall initiated
- Dec 12, 2024
- Classified by FDA
- Jan 14, 2025
- Posted in Enforcement Report
- Jan 22, 2025
- Terminated
- Feb 4, 2025
- Recalling firm
- WHOLESALE PRODUCE SUPPLY LLC DBA
- Firm location
- Minneapolis, MN, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Cucumbers may be contaminated with Salmonella.
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Dec 12, 2024. FDA classified it 33 days later, on Jan 14, 2025. Distribution reported by FDA: IA, IL, KS, MN, MT, ND, NE, SD, WI and Canada WHOLESALE PRODUCE SUPPLY LLC DBA has 2 recalls in our records.
Recalled products (1)
F-0400-2025 Class I Terminated
Cucumbers, Wholesale Produce Supply, 752 Kasota Circle, Minneapolis, MN 554145. Product of Mexico. Cucumbers sold in the following pack sizes: 1. 5 lb. pack 2. 6 ct individual items per case. 3. 12 ct individual items per case. 4. 24 ct individual items per case. 5. 36 ct individual items per case.
Codes / lots: Pack Date: 79 24353 Lot 542547
Quantity: 1178 units
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 96040
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.