RecallHawk
Class I Recall

"Mighty Sesame 10.9oz Organic Tahini" in a 10.9oz plastic squeeze bottle, 8 Units per Cases .

Kenover Marketing Corp.

Summary

The FDA issued a Class I for "Mighty Sesame 10.9oz Organic Tahini" in a 10.9oz plastic squeeze bottle, 8 Unit by Kenover Marketing Corp.. Reason: Kenover Marketing, 72 New Hook, Bayonne NJ, 07002, has initiated a recall of Mighty Sesame 10.9 Oz Organic Tahini (Squeezable), Squeezable Plastic J.

Details

Source

Food Recall

External ID

F-1811-2022

Action Date

2022-10-12

Status

Terminated

Category

food

Product Description

"Mighty Sesame 10.9oz Organic Tahini" in a 10.9oz plastic squeeze bottle, 8 Units per Cases .

Lot/Code Info: UPC: 858313006208 Expiration Date: 3/28/23

Quantity Affected: 1722 cases (8, 10.9oz units/case) = 13,766 units

Reason for Recall

Kenover Marketing, 72 New Hook, Bayonne NJ, 07002, has initiated a recall of Mighty Sesame 10.9 Oz Organic Tahini (Squeezable), Squeezable Plastic Jar, 8 Units per Case, UPC: 858313006208 Expiration Date: 3/28/23 because the product is potentially contaminated with Salmonella.

Distribution

Product was distributed to stores located in MD,NJ,NY, MS,NC, PA, TX, CA, NH, LA, FL, WI, IA,TN,AZ , OR,GA KY, KS,WI and CO.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-08-23

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 57 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-1811-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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