Marketside Fresh Cut Cucumber Slices
Reason Sliced cucumbers have the potential to be contaminated with Salmonella.
Fresh cut cucumber slices recall
Recalled by Walmart Inc · Bentonville, AR, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Potential Salmonella contamination.
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
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
Quantity: 522 units based on point of sale information at stores
Food: Cucumbers
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
00262969000006., all date codes up to 5/24/25
Where it was sold
Texas
FDA's distribution note: 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
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Walmart Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 20, 2025
- In FDA report of
- Jun 11, 2025
- Terminated
- Jun 17, 2025
- FDA recall number
- H-0003-2025 · event 96932
- Official record
- FDA enforcement report search
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