ACTIVE RECALL — CLASS IActive recallH-0249-2026/FDA enforcement
Byheart, INC.·Food·Nov 8, 2025

1

What you need to know

Class I
  • What happened

    Contaminated with Clostridium botulinum

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. Clostridium botulinum can produce a severe neurotoxin in improperly processed or stored food.

  • 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.

Active recall · classified by the FDANationwide (US)More food

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Product identification

Source: FDA FOOD

Brand nameByheart, INC.
Recalling firmByheart, INC.New York, NY, United States
UPC / barcodes
8 50044 96800 800 850044 96889 300 850044 96805 38 50044 96802 28 500449 68015 1
Lot / date codes
  • All batches and codes within expiry Finished Product Quantity 08NOV2023 to 08NOV2025 UPC Codes: Single Can: 8 50044 96800 8
  • Sams Club 2PK: 00850044968893
  • Amazon 2PK: 00850044968053
  • Anywhere pack: 8 50044 96802 2
  • 1-Count Sample Unit Anywhere Pack: 850044968015
Distribution area
Nationwide

nationwide

United States

Quantity affected3, 482, 131 Cans and 3, 531, 901 Single Serve Packets.
Recall initiationFDA report date: December 17, 2025
FDA recall numberH-0249-2026

Beyond the headline

The recall, in context

Byheart, INC. initiated this food recall on November 8, 2025. The FDA enforcement report states: Contaminated with Clostridium botulinum. The FDA report lists distribution as: nationwide.

The FDA enforcement report describes the reason as: Contaminated with Clostridium botulinum

1 was made or distributed by Byheart, INC. in New York, NY, United States. This page reflects FDA report H-0249-2026, dated December 17, 2025.

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, clostridium botulinum can produce a severe neurotoxin in improperly processed or stored food.

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 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

Botulism

Symptoms to watch for

Possible blurred or double vision, drooping eyelids, slurred speech, difficulty swallowing, muscle weakness and breathing difficulty. Seek urgent medical care for these symptoms.

When symptoms may appear

Neurological symptoms typically begin 12 to 36 hours after exposure, but can appear sooner or later.

Higher-risk groups

Infants, older adults, pregnant people and people with weakened immune systems are especially vulnerable.

What to do now

  1. 1Do not taste, eat or use the affected product, even if it looks or smells normal.
  2. 2Seek urgent medical care immediately if anyone has neurological or breathing symptoms; do not wait for test results.
  3. 3Keep the product packaging and contact the recalling firm or retailer about a refund or safe disposal.

Botulism is a medical emergency. Contact emergency services for breathing or neurological symptoms.

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 1 recall?

Byheart, INC. recalled 1 in an FDA Class I enforcement action reported as H-0249-2026. Contaminated with Clostridium botulinum

What are the symptoms of Botulism exposure?

Possible blurred or double vision, drooping eyelids, slurred speech, difficulty swallowing, muscle weakness and breathing difficulty. Seek urgent medical care for these symptoms.

How quickly can Botulism symptoms appear?

Neurological symptoms typically begin 12 to 36 hours after exposure, but can appear sooner or later.

Who is most at risk from Botulism?

Infants, older adults, pregnant people and people with weakened immune systems are especially vulnerable.

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. Do not taste, eat or use the affected product, even if it looks or smells normal. Seek urgent medical care immediately if anyone has neurological or breathing symptoms; do not wait for test results. Keep the product packaging and contact the recalling firm or retailer about a refund or safe disposal.

How do I get a refund from Byheart, INC.?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall H-0249-2026 and keep the packaging, lot code and proof of purchase if you have them.

Is the Byheart, INC. 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 H-0249-2026. 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.