Soom Foods Recall: Soom Foods is recalling its tahini and chocolate tahini halva spread because their manufacturer, Achdut LTD. is recalling its Tahini products of all packages and sizes produced in the following dates: April 7th to May 21st 2018, due to a possible contamination of Salmonella.

🇺🇸 United States

1. November 26, 2018 - Recall initiated
2. February 13, 2019 - Reported by source
3. June 27, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0781-2019

Event ID

81777

Status

Terminated

Classification

Class I

Company

Soom Foods

Product description

Soom Foods Tahini: Soom Sesame Premium Tahini, Single Source Origin, 100 % Roasted and Pressed Sesame Seeds, 11 oz. (6/case or 24/case)

Quantity

900 6 Pack Cases -11oz , 320 24 Pack Cases - 11oz ,

Reason

Soom Foods is recalling its tahini and chocolate tahini halva spread because their manufacturer, Achdut LTD. is recalling its Tahini products of all packages and sizes produced in the following dates: April 7th to May 21st 2018, due to a possible contamination of Salmonella.

Recall initiation date

November 26, 2018

Report date

February 13, 2019

Classification date

Not published in this source record

Termination date

June 27, 2019

Distribution pattern

The Soom Tahini products were distributed throughout the United States, through distributors, retailers, subscription box companies and via Amazon .com.

UPC, lot, and code information

Lot #'s 18-109, 18-119, 18-123

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 81777 with 1 other product entry in Public Health Trace.

Responsible company: Soom Foods

Other recalls from Soom Foods

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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