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
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
Hampstead, MD
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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