Raw cucumbers packaged in cardboard boxes or plastic boxes (RPC) with "SunFed", "Vegetables", or "Agrotato" labeling.
Summary
The FDA issued a Class I for Raw cucumbers packaged in cardboard boxes or plastic boxes (RPC) with "SunFed", by SunFed Produce, Inc.. Reason: Cucumbers potentially contaminated with Salmonella..
Details
Source
Food Recall
External ID
F-0313-2025
Action Date
2025-01-01
Status
Terminated
Category
food
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
Lot/Code Info: No codes
Quantity 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
Reason for Recall
Cucumbers potentially contaminated with Salmonella.
Distribution
National and Foreign distribution
Type: Voluntary: Firm initiated
Recall Initiated: 2024-11-26
Company
Rio Rico, AZ
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (SunFed Produce, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does SunFed Produce, Inc. have FDA actions?
This is the only FDA action we have on record for SunFed Produce, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0313-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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