Yo!man Cucumber
Reason Product contains undeclared cyclamates.
Whole Cucumber bulk cardboard boxes recall
Recalled by Fresh Start Produce Sales, Inc. · Delray Beach, FL, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Due to Salmonella in Cucumbers
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Whole Cucumber, bulk cardboard boxes, 1 1/9 Bu, 60-72 ct cucumbers per box, 24ct box, Carton 36 ct box. Packaged in cardboard container box, color brown with Green and Red inked Accent colors. Grown and Packed by Bedner Growers, INC & Distributed by Fresh Start Produce Sales, Inc listed on sides of the box.
Quantity: 6167 cases of cucumbers
Food: Cucumbers
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Expiration Date 5/27 Lot Number BG0813804
Where it was sold
Florida North Carolina New Jersey Pennsylvania
FDA's distribution note: The product has been distributed in the following States: FL, NJ, PA, and NC
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Fresh Start Produce Sales, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 23, 2024
- In FDA report of
- Jun 26, 2024
- Terminated
- Sep 25, 2024
- FDA recall number
- F-1371-2024 · event 94746
- Official record
- FDA enforcement report search
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