CLASS I Food recall · Reported 3 Aug 2022 · FDA Enforcement Report

Za'atar Seasoning, Cust Part # recalled by Fuchs North America

Fuchs North America is recalling Za'atar Seasoning, Cust Part #, distributed in Pennsylvania. The recall was initiated on 27 Jun 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesGT74862 Lot code: 252491
Quantity recalled700 lbs Za'atar Seasoning, 14 boxes @ 50 lbs each

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1507-2022
FDA event ID
90562
Recalling firm
Fuchs North America, Hampstead, MD
Brand
Za'atar
Classification
Class I
Status
Terminated
Recall initiated
27 Jun 2022
FDA classified
26 Jul 2022
Reported
3 Aug 2022
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Salmonella
Product category
Fish

Timeline

27 Jun 2022Recall initiated by company
26 Jul 2022Classified by FDA+29 days
3 Aug 2022Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

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.

Where it was distributed

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

Pennsylvania

Questions about this recall

Why was it recalled?

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

Which lots are affected?

GT74862 Lot code: 252491

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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