Class ITerminatedVoluntary: Firm initiated
SunFed Produce, Inc.: food recall F-0313-2025
SunFed Produce, Inc. of Rio Rico, AZ recalled Raw cucumbers packaged in cardboard boxes or plastic boxes (RPC) with "SunFed", "Vegetables", or "Agrotato" labeling.… Reason: Cucumbers potentially contaminated with Salmonella. The FDA listed it as Class I in its Enforcement Report dated Jan 1, 2025.
Record status as published: Terminated (terminated Feb 21, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Raw cucumbers packaged in cardboard boxes or plastic boxes (RPC) with "SunFed", "Vegetables", or "Agrotato" labeling. 1 1/9 BU CAS Super Slicer Cucumber/10814780010749 1 1/9 BU CAS Select Slicer Cucumber/10814780010756 1 1/9 BU CAS Large Slicer Cucumber/10814780010763 1 1/9 BU CAS Small Slicer Cucumber/10814780010770 54'S Case Slicer Cucumber/10814780010787 1 1/9 BU RPC Super Slicer Cucumber/10814780010794 24'S Case Slicer Cucumber/10814780010800 36'S Case Slicer Cucumber/10814780010817 1 1/9 BU CAS Plain Slicer Cucumber/10814780011630 36 Case Slicer Cucumber/10814780011722 42 Case Slicer Cucumber/10814780011739 RPC Cucumber super select 62/10814780012682 RPC Cucumber select 62/10814780012699
- Product quantity
- 71,070 cases=10841 cases Cuke 24 count, 14496 Cuke 36 count, 171 cases Cuke 42 Count, 30057 cases Cuke 119, 15505 cuke RPC= 71,070 cases
- Reason for recall
- Cucumbers potentially contaminated with Salmonella.
- Codes, lots and dates on the package
- No codes
- Distribution pattern
- National and Foreign distribution
- Recalling firm
- SunFed Produce, Inc., Rio Rico, AZ
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Telephone
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Nov 26, 2024 |
| Classified by the FDA | Dec 20, 2024 |
| Published in the Enforcement Report | Jan 1, 2025 |
| Terminated | Feb 21, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0313-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.