RecallHawk
Class I Recall

Za'atar Seasoning, Cust Part # Lot No. 252491, NET WT 50 lbs bag in a box. One bag per box, GT 74862, Lot code: 25249

Fuchs North America, Inc.

Summary

The FDA issued a Class I for Za'atar Seasoning, Cust Part # Lot No. 252491, NET WT 50 lbs bag in a box. One by Fuchs North America, Inc.. Reason: The product may be potentially positive for Salmonella due to one of the sub-ingredients (oregano) testing positive for Salmonella..

Details

Source

Food Recall

External ID

F-1507-2022

Action Date

2022-08-03

Status

Terminated

Category

food

Product Description

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.

Lot/Code Info: GT74862 Lot code: 252491

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

Reason for Recall

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

Distribution

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

Type: Voluntary: Firm initiated

Recall Initiated: 2022-06-27

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 84 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Fuchs North America, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Fuchs North America, Inc. have FDA actions?

This is the only FDA action we have on record for Fuchs North America, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1507-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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