Yo!man Cucumber
Reason Product contains undeclared cyclamates.
Cucumber recall
Recalled by Grocery Delivery E-Services USA, Inc. · Richmond, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Firm was notified by their supplier that cucumbers provided are under recall due to potential Salmonella contamination.
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, Super Select Unspecified variety packed in Hello Fresh box the week of August 24-28-2015 in the meal Spicy Tuna Tar-Tacos with Creamy Avocado and Cucumber Radish Slaw. 7-10 inches long, I cucumber per box.
Quantity: 5991 cucumbers
Food: Cucumbers Seafood & fish
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.
ASYS# 5901807; PSYS # 684780 Lot 201508
Where it was sold
Arizona California Idaho Montana Nevada Oregon Utah Washington Wyoming
FDA's distribution note: CA, WA, UT, MT, OR, NV, ID, AZ, WY
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
- Grocery Delivery E-Services USA, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 6, 2015
- In FDA report of
- Nov 25, 2015
- Terminated
- Dec 14, 2015
- FDA recall number
- F-0213-2016 · event 72140
- Official record
- FDA enforcement report search
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