RecallHawk
Class III Recall

Asli Sesame Seeds Brown 14oz., UPC: 7 03440 18270 0; 20 units per wholesale case.

Sands Impex Inc. Dba Asli Fine Foods

Summary

The FDA issued a Class III for Asli Sesame Seeds Brown 14oz., UPC: 7 03440 18270 0; 20 units per wholesale case by Sands Impex Inc. Dba Asli Fine Foods. Reason: Product sample exceeded tolerance for pesticide Fenvalerate.

Details

Source

Food Recall

External ID

F-1489-2024

Action Date

2024-07-24

Status

Terminated

Category

food

Product Description

Asli Sesame Seeds Brown 14oz., UPC: 7 03440 18270 0; 20 units per wholesale case.

Lot/Code Info: Lot Number: 2210-173

Quantity Affected: 28 cases

Reason for Recall

Product sample exceeded tolerance for pesticide Fenvalerate

Distribution

IL, IN, NE, CO, KS, OH, SD, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2024-06-25

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 47 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Sands Impex Inc. Dba Asli Fine Foods has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (Sands Impex Inc. Dba Asli Fine Foods) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Sands Impex Inc. Dba Asli Fine Foods have FDA actions?

Sands Impex Inc. Dba Asli Fine Foods has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1489-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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