Walmart Inc food recall: Fresh cut cucumber slices
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 96932
- Recall initiated
- May 20, 2025
- Classified by FDA
- Jun 3, 2025
- Posted in Enforcement Report
- Jun 11, 2025
- Terminated
- Jun 17, 2025
- Recalling firm
- Walmart Inc
- Firm location
- Bentonville, AR, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- 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
Potential Salmonella contamination.
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 May 20, 2025. FDA classified it 14 days later, on Jun 3, 2025. Distribution reported by FDA: 12 Retail locations in Texas: Ennis, TX; Palestine, TX; Longview, TX; Benbrook/Ft. Worth, TX; Wichita Falls, TX; Frisco Stonebrook, TX; Longview (SE), TX; Saginaw, TX; Rockwall, TX; Lindale, TX; Irving, TX; Paris, TX Walmart Inc has 18 recalls in our records.
Recalled products (1)
H-0003-2025 Class I Terminated
Fresh cut cucumber slices, Marketside, packaged in clear plastic circular container with clear plastic lid and white adhesive label with black print, Walmart, Inc. Bentonville, AR 72716
Codes / lots: 00262969000006., all date codes up to 5/24/25
Quantity: 522 units based on point of sale information at stores
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 96932
- 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.