Kroger Broccoli Raisin Salad Recall: Listeria Contamination Risk
Kroger recalls broccoli raisin salad potentially contaminated with Listeria monocytogenes. Consumers should check UPC codes and follow safety steps to avoid foodborne illness.
Stop using this now
Firm was notified by their supplier that the product may be contaminated with Listeria monocytogenes.
Contact the company
What happened, in plain English
Kro: The Kroger Co is recalling broccoli raisin salad that may contain Listeria monocytogenes. This bacteria can cause serious food poisoning, so affected consumers should stop using the product. Read more at govinfonow.com/recall/24482-kroger-broccoli-raisin-salad-recall-listeria-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/24482-kroger-broccoli-raisin-salad-recall-listeria-contamination-risk · Updated August 10, 2026 · FDA enforcement record: FDA #F-2306-2016
Cite this page
“Kroger Broccoli Raisin Salad Recall: Listeria Contamination Risk.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/24482-kroger-broccoli-raisin-salad-recall-listeria-contamination-risk. Based on FDA recall #F-2306-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2306-2016%22&limit=1).
Why it’s dangerous
Listeria monocytogenes is a bacteria that can cause severe food poisoning. It grows in refrigerated foods and can lead to serious infections, especially in pregnant women, newborns, and people with weakened immune systems.
Who’s affected
Anyone who purchased the Kroger Broccoli Raisin Salad from stores or online. People with weakened immune systems are at higher risk for severe illness.
How to tell if you have this one
Check for the UPC code 002871 58200 0 on the product label. The product was distributed by The Kroger Co in Cincinnati, Ohio.
- Brand
Kroger- Category
Food
What to do — step by step
Stop Using Product
Discard the Kroger Broccoli Raisin Salad if it has the UPC code 002871 58200 0.
Where it went and when
Where it was distributed
Distributed in 18 states.
FDA distribution: “Product was shipped to the following states: AL, AR, GA, IL, IN, KS, KY, MI, MO, MS, NC, NE, OH, SC, TN, TX, VA & WV.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Arkansas, Georgia, Illinois, Indiana, Kansas, Kentucky, Michigan, Mississippi, Missouri, Nebraska, North Carolina, Ohio, South Carolina, Tennessee, Texas, Virginia, West Virginia.
Recall timeline
FDA terminated this recall 2.3 years after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-2306-2016 (May 6, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2306-2016 to see it in context.
- Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.