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RECALL RECORD — CLASS IRecall closedF-2080-2019/FDA enforcement
Northfork Bison Distributions INC.·Food·Jul 12, 2019

Buffalo Burgers ( 100% Pure Canadian Bison Meat ), NET Weight 16 OZ

What you need to know

Class I

  • What happened

    Out Of The Abundance Of Caution, Northfork Bison Distributions Inc. Is Voluntarily Recalling Bison Burgers & Ground Because Of Potential Contamination By E. Coli: 0121 And 0103.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. Some E. coli strains produce toxins that can cause severe, sometimes bloody diarrhea.

  • Action required

    Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent.

Recall closed · classified by the FDADistribution not listedMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameNorthfork Bison Distributions INC.
Recalling firmNorthfork Bison Distributions INC.Saint-Leonard, Canada
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codesNo lot code listed. Follow the recall notice and check the packaging.
Distribution area

GOODS WERE DISTRIBUTED ACROSS THE STATES OF NEW YORK, NEW JERSEY, PENNSYLVANIA, FLORIDA, MISSOURI, VERMONT, VIRGINIA AND ARIZONA TO DISTRIBUTION, INSTITUTIONS AND RETAIL OUTLETS.

United States

Quantity affected1, 904 BOXES; TOTAL WEIGHT 19, 230 LBS
Recall initiationFDA report date: August 14, 2019
FDA recall numberF-2080-2019

Beyond the headline

The recall, in context

Northfork Bison Distributions INC. initiated this food recall on July 12, 2019. The FDA enforcement report states: Out Of The Abundance Of Caution, Northfork Bison Distributions Inc. Is Voluntarily Recalling Bison Burgers & Ground Because Of Potential Contamination By E. Coli: 0121 And 0103. The FDA report lists distribution as: GOODS WERE DISTRIBUTED ACROSS THE STATES OF NEW YORK, NEW JERSEY, PENNSYLVANIA, FLORIDA, MISSOURI, VERMONT, VIRGINIA AND ARIZONA TO DISTRIBUTION, INSTITUTIONS AND RETAIL OUTLETS.

The FDA enforcement report describes the reason as: Out Of The Abundance Of Caution, Northfork Bison Distributions Inc. Is Voluntarily Recalling Bison Burgers & Ground Because Of Potential Contamination By E. Coli: 0121 And 0103.

Buffalo Burgers ( 100% Pure Canadian Bison Meat ), NET Weight 16 OZ was made or distributed by Northfork Bison Distributions INC. in Saint-Leonard, Canada. This page reflects FDA report F-2080-2019, dated August 14, 2019.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, some E. coli strains produce toxins that can cause severe, sometimes bloody diarrhea.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

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

E. coli

Symptoms to watch for

Severe stomach cramps, diarrhea, vomiting and sometimes a low fever. Bloody diarrhea or signs of dehydration need prompt medical attention.

When symptoms may appear

Usually 3 to 4 days after exposure, with a range of roughly 1 to 10 days.

Higher-risk groups

Young children, older adults, pregnant people and people with weakened immune systems are at higher risk of complications.

What to do now

  1. 1Stop using or eating the affected product and keep it away from children and pets.
  2. 2Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer.
  3. 3If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

General guidance based on CDC and FDA consumer information.

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 Buffalo Burgers ( 100% Pure Canadian Bison Meat ), NET Weight 16 OZ recall?

Northfork Bison Distributions INC. recalled Buffalo Burgers ( 100% Pure Canadian Bison Meat ), NET Weight 16 OZ in an FDA Class I enforcement action reported as F-2080-2019. Out Of The Abundance Of Caution, Northfork Bison Distributions Inc. Is Voluntarily Recalling Bison Burgers & Ground Because Of Potential Contamination By E. Coli: 0121 And 0103.

What should I do if I bought this product?

Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent. Stop using or eating the affected product and keep it away from children and pets. Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer. If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

Is the Northfork Bison Distributions INC. 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-2080-2019. 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.