Cucumbers Pennrose Farms, Net Wt. 5lbs(2.26kg) Mesh bag, Distributed by PennRose Farms, LLC Welington, FL 33414, UPC cod
Summary
The FDA issued a Class I for Cucumbers Pennrose Farms, Net Wt. 5lbs(2.26kg) Mesh bag, Distributed by PennRose by pennrose farms LLC. Reason: Due to potential Salmonella Contamination.
Details
Source
Food Recall
External ID
H-0006-2025
Action Date
2025-06-11
Status
Terminated
Category
food
Product Description
Cucumbers Pennrose Farms, Net Wt. 5lbs(2.26kg) Mesh bag, Distributed by PennRose Farms, LLC Welington, FL 33414, UPC code 841214101714
Lot/Code Info: Lot: 48-122, 48-123, 48-124, 48-125 best by date: 5/12/24 packaged between May 2-May 5
Quantity Affected: 1,152 cases or 9,216 individual units (bags)
Reason for Recall
Due to potential Salmonella Contamination
Distribution
Product was shipped to FL, NJ, GA, IL, OH
Type: Voluntary: Firm initiated
Recall Initiated: 2025-05-20
Company
Wellington, FL
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 123 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 (pennrose farms LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does pennrose farms LLC have FDA actions?
This is the only FDA action we have on record for pennrose farms LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0006-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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