Tainy Vostoka brand Assorted Dry Fruits-Apple
Reason NYS found elevated levels of undeclared Sulfites in Tainy Vostoka Assorted Dry Fruits - Apple.
Capitan K Salmon slightly salted piece recall
Recalled by Euphoria Fancy Food Inc · Brooklyn, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product may be contaminated with Listeria monocytogenes.
Pathogen: Listeria
Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.
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
Capitan K Salmon slightly salted piece - net.wt 1.05 oz (200g) Distributed by: Euphoria Fancy Food Inc. 149-151 2nd avenue Brooklyn, New York 11215, USA Product of Russia UPC: 607059000362
Quantity: 24 Cases
Food: 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.
Best By Dates: 01/05/20, 01/30/20, 02/02/20, 02/12/20 UPC: 607059000362
Where it was sold
New Jersey New York Pennsylvania Washington
FDA's distribution note: Product was distributed in NY, PA, NJ & WA
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
- Euphoria Fancy Food Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 20, 2019
- In FDA report of
- Oct 30, 2019
- Terminated
- Feb 11, 2021
- FDA recall number
- F-0072-2020 · event 83876
- Official record
- FDA enforcement report search
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