Aleppo Tahini Sesame Paste, 32oz, Plastic jar, 1lb (16oz), 12 per case
Summary
The FDA issued a Class I for Aleppo Tahini Sesame Paste, 32oz, Plastic jar, 1lb (16oz), 12 per case by Turkana Food Inc.. Reason: Product tested positive for Salmonella.
Details
Source
Food Recall
External ID
F-0609-2025
Action Date
2025-03-19
Status
Terminated
Category
food
Product Description
Aleppo Tahini Sesame Paste, 32oz, Plastic jar, 1lb (16oz), 12 per case
Lot/Code Info: LOT # 120824-01
Quantity Affected: 858 cases total 12 jars per case
Reason for Recall
Product tested positive for Salmonella
Distribution
The recalled product was distributed to the following States: AL, CA, CO, DE, FL, GA, IL, IN, KY, MD, MA, MI, MO, NC, NJ, NY, OH, PA, RI, TN, TX, VA, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2025-01-31
Company
Kenilworth, NJ
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 55 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Turkana Food Inc. has 4 FDA actions in our database, including 4 recalls.
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 (Turkana Food Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Turkana Food Inc. have FDA actions?
Turkana Food Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0609-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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