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RECALL RECORD — CLASS IRecall closedF-0291-2023/FDA enforcement
Byheart, INC.·Food·Dec 11, 2022

By Heart Whole Nutrition Infant Formula, NET WT

What you need to know

Class I

  • What happened

    Infant formula potentially contaminated with Cronobacter sakazakii

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. Cronobacter bacteria can cause severe illness, especially in infants and premature babies.

  • 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 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
19589362296
Lot / date codes
  • Packaged between September 30, 2022 and October 07, 2022 printed with following codes: 22273 C1, 22276 C1, 22277 C1, 22278 C1, and 22280 C1 with best by 01 JAN 24 or 01 JUL 24 or 01SEP24 UPC Codes: 19589362296
Distribution area
Nationwide

nationwide direct to consumer subscription e-commerce sales

United States

Quantity affected28, 554 cans
Recall initiationFDA report date: January 25, 2023
FDA recall numberF-0291-2023

Beyond the headline

The recall, in context

Byheart, INC. initiated this food recall on December 11, 2022. The FDA enforcement report states: Infant formula potentially contaminated with Cronobacter sakazakii. The FDA report lists distribution as: nationwide direct to consumer subscription e-commerce sales.

The FDA enforcement report describes the reason as: Infant formula potentially contaminated with Cronobacter sakazakii

By Heart Whole Nutrition Infant Formula, NET WT was made or distributed by Byheart, INC. in New York, NY, United States. This page reflects FDA report F-0291-2023, dated January 25, 2023.

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, cronobacter bacteria can cause severe illness, especially in infants and premature babies.

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

Cronobacter

Symptoms to watch for

In infants, possible poor feeding, irritability, temperature changes, jaundice, grunting or seizures. In adults, fever and gastrointestinal symptoms may occur.

When symptoms may appear

The timing varies; infant infections can become serious quickly.

Higher-risk groups

Infants, especially premature or low-birth-weight babies, and immunocompromised people are at highest risk.

What to do now

  1. 1Do not feed the affected product to an infant or anyone in a high-risk group.
  2. 2If an infant has poor feeding, unusual irritability, fever or breathing problems, seek urgent medical care.
  3. 3Keep the packaging, contact the retailer or manufacturer for a refund, and follow the recall notice for safe disposal.

Powdered infant formula and infant-feeding products warrant extra caution.

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 By Heart Whole Nutrition Infant Formula, NET WT recall?

Byheart, INC. recalled By Heart Whole Nutrition Infant Formula, NET WT in an FDA Class I enforcement action reported as F-0291-2023. Infant formula potentially contaminated with Cronobacter sakazakii

What are the symptoms of Cronobacter exposure?

In infants, possible poor feeding, irritability, temperature changes, jaundice, grunting or seizures. In adults, fever and gastrointestinal symptoms may occur.

How quickly can Cronobacter symptoms appear?

The timing varies; infant infections can become serious quickly.

Who is most at risk from Cronobacter?

Infants, especially premature or low-birth-weight babies, and immunocompromised people are at highest risk.

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 feed the affected product to an infant or anyone in a high-risk group. If an infant has poor feeding, unusual irritability, fever or breathing problems, seek urgent medical care. Keep the packaging, contact the retailer or manufacturer for a refund, and follow the recall notice for 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 F-0291-2023 and keep the packaging, lot code and proof of purchase if you have them.

Is the Byheart, 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-0291-2023. 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.