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RECALL RECORD — CLASS IIRecall closedF-0780-2023/FDA enforcement
Cargill, INC Corporate Headquarters·Food·Mar 30, 2023

Prosante Tsoyflr 3018p Flk 50lb Bg, Prosante Tsoyflr 3018p Flk 50lb Bg 18/p, Prosante Tsoyflr…

What you need to know

Class II

  • What happened

    Products with a gluten free claim may contain gluten levels above 20 ppm.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • 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.

Recall closed · classified by the FDANationwide (US)More food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameCargill, INC Corporate Headquarters
Recalling firmCargill, INC Corporate HeadquartersWayzata, MN, United States
UPC / barcodes
10 000135 10032 310 000135 10042 310 000135 10102 310 000135 12842 211 002377 70022 311 002377 70052 311 002377 70062 311 002377 70112 311 002377 70132 311 002377 70312 311 002377 70322 311 002377 70332 3
Lot / date codes
  • 100001351-00323CHXEA 100001351-00423CHXEA 100001351-01023CHXEA 100001351-28422CHXEA 110023777-00223CHXEA 110023777-00523CHXEA 110023777-00623CHXEA 110023777-01123CHXEA 110023777-01323CHXEA 110023777-03123CHXEA 110023777-03223CHXEA 110023777-03323CHXEA 110023777-05223CHXEA 110023777-05323CHXEA 110023777-05423CHXEA 110023777-05823CHXEA 110023777-05923CHXEA 110023777-06123CHXEA 110023777-27822CHXEA 110023777-27922CHXEA 110023777-28422CHXEA 110023777-28522CHXEA 110023777-28622CHXEA 110023777-28722CHXEA 110023777-29722CHXEA 110023777-29822CHXEA 110023777-30022CHXEA 110023777-32122CHXEA 110023777-33322CHXEA 110023777-33522CHXEA 110023777-36222CHXEA 110023777-36322CHXEA 110023777-36422CHXEA 100001351-31922CHXEA 100001351-32022CHXEA 100001351-33222CHXEA 100001351-33322CHXEA 110026502-00923CHXEA 110026502-03023CHXEA 110026502-07223CHXEA 110026502-28322CHXEA 110026502-29722CHXEA 110026502-29922CHXEA 110026502-31822CHXEA 110026502-31922CHXEA 110026502-33222CHXEA 110026502-36222CHXEA
Distribution area
Nationwide

Nationwide United States, Canada, Chile, Costa Rica, Guatemala, Mexico, and United Kingdom

United States, Canada, Mexico, United Kingdom

Quantity affected977, 000 lbs
Recall initiationFDA report date: May 10, 2023
FDA recall numberF-0780-2023

Beyond the headline

The recall, in context

Cargill, INC Corporate Headquarters initiated this food recall on March 30, 2023. The FDA enforcement report states: Products with a gluten free claim may contain gluten levels above 20 ppm. The FDA report lists distribution as: Nationwide United States, Canada, Chile, Costa Rica, Guatemala, Mexico, and United Kingdom.

The FDA enforcement report describes the reason as: Products with a gluten free claim may contain gluten levels above 20 ppm.

Prosante Tsoyflr 3018p Flk 50lb Bg, Prosante Tsoyflr 3018p Flk 50lb Bg 18/p, Prosante Tsoyflr… was made or distributed by Cargill, INC Corporate Headquarters in Wayzata, MN, United States. This page reflects FDA report F-0780-2023, dated May 10, 2023.

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, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

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 UPC and lot code 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

Undeclared wheat or gluten

Symptoms to watch for

Wheat allergy can cause hives, nausea, cramps, breathing difficulty or anaphylaxis. For celiac disease, even small amounts of gluten can cause intestinal damage.

When symptoms may appear

Allergic reactions can begin within minutes to hours. Celiac-related intestinal effects may be delayed.

Higher-risk groups

People with wheat allergy, celiac disease, non-celiac gluten sensitivity or a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a wheat allergy or must avoid gluten.
  2. 2Seek emergency care for breathing difficulty or other signs of a severe allergic reaction.
  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 Prosante Tsoyflr 3018p Flk 50lb Bg, Prosante Tsoyflr 3018p Flk 50lb Bg 18/p, Prosante Tsoyflr… recall?

Cargill, INC Corporate Headquarters recalled Prosante Tsoyflr 3018p Flk 50lb Bg, Prosante Tsoyflr 3018p Flk 50lb Bg 18/p, Prosante Tsoyflr… in an FDA Class II enforcement action reported as F-0780-2023. Products with a gluten free claim may contain gluten levels above 20 ppm.

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. Do not eat the product if you have a wheat allergy or must avoid gluten. Seek emergency care for breathing difficulty or other signs of a severe allergic reaction. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Cargill, INC Corporate Headquarters recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0780-2023. 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

Brand history

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