RecallHawk
Class II Recall

Fancy Buckwheat Flour, Item #327, 50 lbs. net wt, Packed by Min-Dak Growers Grand Forks, ND - Product of the USA. Manu

Minn Dak Growers, Ltd.

Summary

The FDA issued a Class II for Fancy Buckwheat Flour, Item #327, 50 lbs. net wt, Packed by Min-Dak Growers Gra by Minn Dak Growers, Ltd.. Reason: Foreign Material - plastic.

Details

Source

Food Recall

External ID

F-1561-2022

Action Date

2022-08-24

Status

Ongoing

Category

food

Product Description

Fancy Buckwheat Flour, Item #327, 50 lbs. net wt, Packed by Min-Dak Growers Grand Forks, ND - Product of the USA. Manufactured for Enjoy Life Foods.

Lot/Code Info: Lot: 010622, Expiration Date: 01-10-24 and Lot : 011022, Expiration Date 01-06-24

Quantity Affected: 40,000 lbs.

Reason for Recall

Foreign Material - plastic

Distribution

IN

Type: Voluntary: Firm initiated

Recall Initiated: 2022-07-18

Company

Minn Dak Growers, Ltd.

Grand Forks, ND

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 38 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 (Minn Dak Growers, Ltd.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Minn Dak Growers, Ltd. have FDA actions?

This is the only FDA action we have on record for Minn Dak Growers, Ltd. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1561-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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