Food Recall Check
Class I · High risk Terminated Initiated Feb 25, 2021 (6 years ago)

Tahina Sesame Paste packaged in recall

Recalled by Kareem Mart INC · Garden City, MI, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Product tested positive for Salmonella.

Pathogen: Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

Tahina Sesame Paste packaged in 1lb and 2lb plastic jars and 10kg metal containers; UPC CODES 6215000382207

Quantity: 1800 of the 1lb units; 450 of the 2lb units; and 100 of the 10kg units

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot 1, DATE OF EXPIRATION 07-01-2022, numbers in firm systems are KH100P045, KH100P090, KH100M100

Where it was sold

Illinois Michigan Montana North Carolina New York Ohio Pennsylvania Virginia

FDA's distribution note: The products covered by this recall may have been distributed to a distributor and retail stores in the following states: Illinois, Montana, Michigan, New York, North Carolina, Ohio, Pennsylvania, and Virginia.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Kareem Mart INC
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 25, 2021
In FDA report of
Mar 24, 2021
Terminated
Sep 1, 2021
FDA recall number
F-0341-2021 · event 87438
Official record
FDA enforcement report search

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