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ACTIVE RECALL — CLASS IIActive recallF-1561-2022/FDA enforcement
Minn Dak Growers, LTD.·Food·Jul 18, 2022

Fancy Buckwheat Flour, Item #327, 50 Lbs

What you need to know

Class II

  • What happened

    Foreign Material - plastic

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Plastic fragments can pose a choking risk or irritate and injure the digestive tract.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Active recall · classified by the FDAINMore food

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Product identification

Source: FDA FOOD

Brand nameMinn Dak Growers, LTD.
Recalling firmMinn Dak Growers, LTD.Grand Forks, ND, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot: 010622, Expiration Date: 01-10-24 and Lot : 011022, Expiration Date 01-06-24
Distribution area
IN

IN

United States

Quantity affected40, 000 lbs.
Recall initiationFDA report date: August 24, 2022
FDA recall numberF-1561-2022

Beyond the headline

The recall, in context

Minn Dak Growers, LTD. initiated this food recall on July 18, 2022. The FDA enforcement report states: Foreign Material - plastic. The FDA report lists distribution as: IN.

The FDA enforcement report describes the reason as: Foreign Material - plastic

Fancy Buckwheat Flour, Item #327, 50 Lbs was made or distributed by Minn Dak Growers, LTD. in Grand Forks, ND, United States. This page reflects FDA report F-1561-2022, dated August 24, 2022.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, plastic fragments can pose a choking risk or irritate and injure the digestive tract.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Plastic contamination

Possible health effects

Plastic fragments can pose a choking risk or cause irritation or injury to the mouth and digestive tract.

Higher-risk groups

Young children and anyone who may swallow a fragment without noticing are at greater risk.

What to do now

  1. 1Stop eating or using the product and do not taste or chew it to check for fragments.
  2. 2Seek medical care if anyone has swallowed plastic or has breathing difficulty, severe pain or persistent vomiting.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Fancy Buckwheat Flour, Item #327, 50 Lbs recall?

Minn Dak Growers, LTD. recalled Fancy Buckwheat Flour, Item #327, 50 Lbs in an FDA Class II enforcement action reported as F-1561-2022. Foreign Material - plastic

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop eating or using the product and do not taste or chew it to check for fragments. Seek medical care if anyone has swallowed plastic or has breathing difficulty, severe pain or persistent vomiting. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Minn Dak Growers, LTD. recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1561-2022. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.