FDA Food recall ·

Raw cucumbers packaged in cardboard boxes or plastic boxes (RPC) with… recall

This is an FDA Class I recall — the most serious type.

Recall number
F-0313-2025
Date
(initiated November 26, 2024)
Company / brand
SunFed Produce, Inc.
51 Kipper St, Rio Rico, AZ, United States
Category
Food › Class I
Classification
Class I
Status
Terminated
Units affected
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
Hazard tags
Salmonella Microbial contamination
Initiated by
Voluntary: Firm initiated

Read the official FDA notice ↗

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

Why was it recalled?

Cucumbers potentially contaminated with Salmonella.

What should you do?

FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.

Product codes & lot numbers

No codes

Distribution

National and Foreign distribution

What does Class I mean?

Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.

Source: FDA (food), recall F-0313-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.