Whole select cucumbers, 1/2 bushel, packed in a generic cardboard box, labeled as CUCUMBER Grn Ctn 24ct Box Packed By: A
Summary
The FDA issued a Class I for Whole select cucumbers, 1/2 bushel, packed in a generic cardboard box, labeled a by Alex Kontos/Flavor-Pic Tomato Company. Reason: Product has potential contamination with Salmonella.
Details
Source
Food Recall
External ID
H-0013-2025
Action Date
2025-06-11
Status
Terminated
Category
food
Product Description
Whole select cucumbers, 1/2 bushel, packed in a generic cardboard box, labeled as CUCUMBER Grn Ctn 24ct Box Packed By: Alex Kontos Fruit Co., Inc. Birmingham, AL
Lot/Code Info: GTIN: 70095175008424; Lot Number: 3-182769; Pack Date: May07; Internal Item: 2320
Quantity Affected: 20 cases
Reason for Recall
Product has potential contamination with Salmonella
Distribution
One (1) distributor in: KY
Type: Voluntary: Firm initiated
Recall Initiated: 2025-05-21
Company
Birmingham, AL
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 (Alex Kontos/Flavor-Pic Tomato Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Alex Kontos/Flavor-Pic Tomato Company have FDA actions?
This is the only FDA action we have on record for Alex Kontos/Flavor-Pic Tomato Company in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0013-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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