Food Recall Check
Class I · High risk Terminated Initiated Aug 20, 2015 (11 years ago)

Deep All Natural Spices Coriander Powder recall

Recalled by Chetak New York, LLC · Edison, NJ, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Chetak New York L.L.C. of Edison, NJ is recalling 300 jars of 14.1oz Deep Coriander Powder, Lot# LE15152, because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

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

Deep All Natural Spices Coriander Powder, Net Wt 400g/14.1 oz Product of India, Distributed by: Chetak New York, L.L.C. Edison, NJ 08837 USA

Quantity: 300 - 14.1 ounce plastic containers.

Food: Spices & seasonings

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.

UPC #011433134347; Lot: LE15152

Where it was sold

Nationwide.

FDA's distribution note: Nationwide

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
Chetak New York, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 20, 2015
In FDA report of
Sep 9, 2015
Terminated
Jun 14, 2017
FDA recall number
F-3078-2015 · event 72014
Official record
FDA enforcement report search

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