Yo!man Cucumber
Reason Product contains undeclared cyclamates.
Raw Refrigerated Cucumbers recall
Recalled by Maglio & Co Ready Fresh · Glendale, WI, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
A sample of raw cucumbers tested positive for Salmonella spp.
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
Raw Refrigerated Cucumbers, 11/9 bushel, 6 count, 12 count, 24 count, in corrugated cardboard cases, Southern Valley Produce Lot 16300705. (The product was either distributed in original container or were repackaged).
Quantity: 2150 pounds
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.
" X0882402 " X0882328 " X0882419 " X0882663 " X0882664 " X0882776 " X0882415 " X0882808 " X0035508 " X0035548 " X0035583 " X0882379 " X0882385 " X0882465 " X0882875 " X0882585 " X0882562 " X0882849
Where it was sold
Michigan Minnesota Missouri Nebraska Wisconsin
FDA's distribution note: Il, WI, NE, MO, MI, MN .
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
- Maglio & Co Ready Fresh
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 30, 2016
- In FDA report of
- Aug 17, 2016
- Terminated
- Jul 26, 2017
- FDA recall number
- F-1921-2016 · event 74589
- Official record
- FDA enforcement report search
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