Del Monte Fresh Cut Corn Recall: Post-Process Spoilage Risk
Del Monte recalls 15.25 oz. corn cans with post-process spoilage found during distribution. Consumers should check UPCs and lot numbers for affected products.
Lower-risk recall
Firm discovered that some containers exhibited post-process spoilage during additional inspection and deployment of product at Distribution Center.
Contact the company
What happened, in plain English
Del Monte is recalling fresh cut golden sweet whole kernel corn due to spoilage issues found during distribution. This could lead to unsafe food consumption if the corn is consumed after spoilage occurs. Read more at govinfonow.com/recall/14385-del-monte-fresh-cut-corn-recall-post-process-spoilage-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/14385-del-monte-fresh-cut-corn-recall-post-process-spoilage-risk · Updated October 4, 2026 · FDA enforcement record: FDA #F-0808-2021
Cite this page
“Del Monte Fresh Cut Corn Recall: Post-Process Spoilage Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14385-del-monte-fresh-cut-corn-recall-post-process-spoilage-risk. Based on FDA recall #F-0808-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0808-2021%22&limit=1).
Why it’s dangerous
The recall was initiated after some containers showed post-process spoilage during additional inspections at the distribution center. This spoilage could potentially lead to unsafe food consumption if the corn is consumed after spoilage occurs.
Who’s affected
Consumers who purchased Del Monte Fresh Cut Golden Sweet Whole Kernel Corn in 15.25 oz. cans with specific UPC and lot numbers from March 2024. Those who have the product and are concerned about spoilage are most at risk.
How to tell if you have this one
Check for the UPC 024000163022 on the can and lot numbers from 1064BD to 1070BD, which were distributed starting March 2024.
- Brand
Del Monte- Product
Del Monte Fresh Cut Golden Sweet Whole Kernel Corn; 15.25 oz. can (24 x 15.25 oz. cans per case) Case UPC- Category
Food
What to do — step by step
Check Product Details
Verify the UPC code on the can (024000163022) and lot numbers (1064BD to 1070BD) to confirm if your product is affected.
Where it went and when
Where it was distributed
Distributed in 19 states.
FDA distribution: “AL, AR, IA, IL, IN, KS, KY, LA, MI, MN, MO, MS, ND, NE, OH, PA, TN, WI, WV” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Arkansas, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Michigan, Minnesota, Mississippi, Missouri, Nebraska, North Dakota, Ohio, Pennsylvania, Tennessee, West Virginia, Wisconsin.
Recall timeline
FDA terminated this recall 6 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
What should I do if I have the affected product?
The recall does not require immediate action; check the product details to confirm if it is affected.
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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-0808-2021 (June 22, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0808-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 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.