RecallHawk
Class I Recall

Al'Fez Natural Tahini in 5.6oz glass jars, UPC 711464506778

AB WORLD FOODS US INC

Summary

The FDA issued a Class I for Al'Fez Natural Tahini in 5.6oz glass jars, UPC 711464506778 by AB WORLD FOODS US INC. Reason: Potential to be contaminated with Salmonella.

Details

Source

Food Recall

External ID

F-1654-2024

Action Date

2024-08-14

Status

Terminated

Category

food

Product Description

Al'Fez Natural Tahini in 5.6oz glass jars, UPC 711464506778

Lot/Code Info: Lot 3031, Best Before 2024-07-31 Lot 3080, Best Before 2024-09-21 Lot 3270, Best Before 2025-03-27 Lot 3297, Best Before 2025-04-24

Quantity Affected: 3522 cases

Reason for Recall

Potential to be contaminated with Salmonella

Distribution

Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2024-07-11

Company

AB WORLD FOODS US INC

Oakbrook Terrace, IL

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 200 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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 (AB WORLD FOODS US INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does AB WORLD FOODS US INC have FDA actions?

This is the only FDA action we have on record for AB WORLD FOODS US INC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1654-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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