PRIME TIME Cucumbers
Reason Sun and Sands Enterprise dba Prime Time International is recalling cucumber bushels (Lot 10-1461) because they have the potential to be contaminated with Salmonella.
Cucumber whole recall
Recalled by Prime Time International · Coachella, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Prime Time is recalling cucumber bushels because they have the potential to be contaminated with Salmonella.
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
Cucumber, whole, fresh, 1 1/9 Plain, 1 1/9 Large, 6/10 36's, 5/10 36's Especial, Item#1472554. sold in Tan cardboard case with Red and Green Print. Case reads in part "***CUCUMBERS***PRIME TIME***CUCUMBERS***6/10 BUSHEL
Quantity: 1,119 cartons
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.
Lot 1-2885 Julian date code sticker: 280 Stamp: Agricola Maui
Where it was sold
Arizona California Oregon Pennsylvania
FDA's distribution note: CA, PA, AZ, OR
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
- Prime Time International
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 8, 2016
- In FDA report of
- Dec 14, 2016
- Terminated
- Feb 9, 2017
- FDA recall number
- F-0576-2017 · event 75631
- Official record
- FDA enforcement report search
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