RecallHawk
Class III Recall

Tereos Wheat Gluten, Net Weight 50 lbs, Distributed by Meelunie, Produced in France

Able Sales Company, Inc.

Summary

The FDA issued a Class III for Tereos Wheat Gluten, Net Weight 50 lbs, Distributed by Meelunie, Produced in Fra by Able Sales Company, Inc.. Reason: Traces of 2-chloro-ethanol (2-CE) in wheat gluten..

Details

Source

Food Recall

External ID

F-1082-2022

Action Date

2022-06-01

Status

Terminated

Category

food

Product Description

Tereos Wheat Gluten, Net Weight 50 lbs, Distributed by Meelunie, Produced in France

Lot/Code Info: Batch Numbers: F2I252411 F2I252431 F2I252441 F2I252451 F2J112411 F2J183404 F2J193401 F2J197404 F2J249413 F2J256401

Quantity Affected: 8,000 bags/50 lb each

Reason for Recall

Traces of 2-chloro-ethanol (2-CE) in wheat gluten.

Distribution

Domestic distribution only - PR

Type: Voluntary: Firm initiated

Recall Initiated: 2022-04-05

Company

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

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 (Able Sales Company, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Able Sales Company, Inc. have FDA actions?

This is the only FDA action we have on record for Able Sales Company, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1082-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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