Food Recall Check
Class I · High risk Terminated Initiated Jun 27, 2022 (4 years ago)

Za'atar Seasoning Cust Part # recall

Recalled by Fuchs North America, Inc. · Hampstead, MD, United States

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

Why it was recalled

The product may be potentially positive for Salmonella due to one of the sub-ingredients (oregano) testing positive for 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

Za'atar Seasoning, Cust Part # Lot No. 252491, NET WT 50 lbs bag in a box. One bag per box, GT 74862, Lot code: 252491.

Quantity: 700 lbs Za'atar Seasoning, 14 boxes @ 50 lbs each

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.

GT74862 Lot code: 252491

Where it was sold

Pennsylvania

FDA's distribution note: The product was distributed to one Consignee. That's How We Roll (a Hain Company) 10 Innovation Drive, York, PA 17402

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
Fuchs North America, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 27, 2022
In FDA report of
Aug 3, 2022
Terminated
Oct 17, 2022
FDA recall number
F-1507-2022 · event 90562
Official record
FDA enforcement report search

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