FDA recall record

SunFed Produce "Vegetables", or "Agrotato" labeling recall — FDA F-0313-2025

Cucumbers potentially contaminated with Salmonella.

Class Iclassification
F-0313-2025official record ID
Jan 1, 2025report date

Recall record at a glance

Official recordF-0313-2025
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmSunFed Produce, Inc.
Report dateJan 1, 2025
Recall initiation dateNov 26, 2024
Quantity71,070 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
LocationRio Rico, AZ, United States

Official product description

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

Why the product was recalled

Cucumbers potentially contaminated with Salmonella.

Distribution information

National and Foreign distribution

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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