Food Recall Check
Class I · High risk Terminated Initiated Jul 24, 2014 (12 years ago)

Product is in a 160 gram recall

Recalled by The TJX Companies, Inc. · Framingham, MA, United States

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

Why it was recalled

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

Product is in a 160 gram, light green tin container, labeled in part: "ecoato Sweet Paprika Powder Product of Spain"

Quantity: approx. 150 units

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.

Lot# 8147

Where it was sold

Alabama Connecticut District of Columbia Florida Georgia Illinois Louisiana Massachusetts Maryland Mississippi North Carolina New Hampshire New York Puerto Rico Rhode Island South Carolina Tennessee Texas Virginia

FDA's distribution note: Alabama, Connecticut, Maryland, Massachusetts, Rhode Island, South Carolina, District of Columbia, Mississippi, Tennessee, Florida, New Hampshire, Texas, Georgia, New York, Virginia, Illinois, Louisiana, North Carolina, Puerto Rico

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
The TJX Companies, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 24, 2014
In FDA report of
Aug 27, 2014
Terminated
Oct 7, 2014
FDA recall number
F-2333-2014 · event 68904
Official record
FDA enforcement report search

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