Check the Batch
Class ITerminated in FDA datasetRecall initiated Nov 23, 2018

Raw Tahini sold under the following brand names: Baron's raw Tahini, 454g

Recalling firm: Achdut

Why it was recalled

Product may be contaminated with Salmonella.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 20, 2019.

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Compare the exact product and package details with the label you have.

ProductRaw Tahini sold under the following brand names: Baron's raw Tahini, 454g, UPC: 816412010083; Soom raw Tahini 220kg (no barcode on product); Soom raw Tahini 18kg, UPC: 718088347329; Soom raw Tahini, 454g, UPC: 718088347411
Package size454g
UPC718088347329, 718088347411, 816412010083

FDA code information

18-097 through 18-141

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Raw Tahini sold under the following brand names: Baron's raw Tahini, 454g, UPC: 816412010083; Soom raw Tahini 220kg (no barcode on product); Soom raw Tahini 18kg, UPC: 718088347329; Soom raw Tahini, 454g, UPC: 718088347411

Extracted codes and context

TypeCode / valueContext
UPC7180883473290083; Soom raw Tahini 220kg (no barcode on product); Soom raw Tahini 18kg, UPC: 718088347329; Soom raw Tahini, 454g, UPC: 718088347411
UPC718088347411 product); Soom raw Tahini 18kg, UPC: 718088347329; Soom raw Tahini, 454g, UPC: 718088347411
UPC816412010083Raw Tahini sold under the following brand names: Baron's raw Tahini, 454g, UPC: 816412010083; Soom raw Tahini 220kg (no barcode on product); Soom raw Tahini 18kg, UPC: 718088347329; Soom raw Tahini, 454g, UPC: 71

Original FDA recall reason

Product may be contaminated with Salmonella.

Recall details

Recall number
F-0728-2019
Event ID
81633
FDA status
Terminated
Initiated
Nov 23, 2018
Reported
Dec 26, 2018
Classified
Dec 14, 2018
Terminated
Mar 20, 2019
Quantity
88,490 units (total for all products)
Location
Ari'El, Israel
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Direct to NY, CA, PA and Israel

FDA source record · F-0728-2019

Data updated September 16, 2026. View official FDA data ↗

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