Mighty Sesame 10.9 Oz Organic Tahini (Squeezable) bottle, UPC 858313006208, 8 Units per case.
Summary
The FDA issued a Class I for Mighty Sesame 10.9 Oz Organic Tahini (Squeezable) bottle, UPC 858313006208, 8 Un by Kenover Marketing Corp.. Reason: The product is being recalled due to Salmonella contamination..
Details
Source
Food Recall
External ID
F-0954-2023
Action Date
2023-05-24
Status
Terminated
Category
food
Product Description
Mighty Sesame 10.9 Oz Organic Tahini (Squeezable) bottle, UPC 858313006208, 8 Units per case.
Lot/Code Info: Lot Number 092523, expiration date of 9/25/23
Quantity Affected: 1447 Cases
Reason for Recall
The product is being recalled due to Salmonella contamination.
Distribution
The product was disturbed to the following States. MD, IN, CA, PA, IL, NH, SC, TX, KY, TX, NY, GA, OH, WI, NC, AR, NJ
Type: Voluntary: Firm initiated
Recall Initiated: 2023-05-03
Company
Bayonne, 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 74 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Kenover Marketing Corp. 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 (Kenover Marketing Corp.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Kenover Marketing Corp. have FDA actions?
Kenover Marketing Corp. 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-0954-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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