Cucumbers, Wholesale Produce Supply, Bedner Growers, Inc. 10066 Lee Road Boynton Beach, FL 33473 (561)733-5490. Cucumber
Summary
The FDA issued a Class I for Cucumbers, Wholesale Produce Supply, Bedner Growers, Inc. 10066 Lee Road Boynton by Bedner Growers, Inc.. Reason: Cucumbers may be potentially contaminated with Salmonella.
Details
Source
Food Recall
External ID
H-0002-2025
Action Date
2025-06-11
Status
Terminated
Category
food
Product Description
Cucumbers, Wholesale Produce Supply, Bedner Growers, Inc. 10066 Lee Road Boynton Beach, FL 33473 (561)733-5490. Cucumbers were packaged in cardboard shipping boxes to customers with packaging sizes consisting of 68, 36, or 24 count per box.
Lot/Code Info: Recall includes all cucumbers shipped from May 3- May 12, 2025. Lot numbers: 4/29/2025 BH04-B129 4/30/2025 BH1713004 5/1/2025 BH1713104 5/2/2025 BH0813204 5/3/2025 BH1713304 5/4/2025 BH1713404 5/5/2025 BH0613504 5/6/2025 BH1713604 5/7/2025 BH0813704 5/8/2025 BH0813804 5/10/2025 BH0614004
Quantity Affected: 126,159 cartons
Reason for Recall
Cucumbers may be potentially contaminated with Salmonella
Distribution
Florida
Type: Voluntary: Firm initiated
Recall Initiated: 2025-05-16
Company
Boynton Beach, 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 (Bedner Growers, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Bedner Growers, Inc. have FDA actions?
This is the only FDA action we have on record for Bedner Growers, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0002-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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