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ACTIVE RECALL — CLASS IActive recallF-0949-2022/FDA enforcement
Abbott Laboratories·Dietary Supplements·Feb 17, 2022

Abbott Elecare Amino Acid-based Powder Infant Formula with Iron 14.1oz

What you need to know

Class I

  • What happened

    Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had…

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A bacteria commonly linked to poultry, eggs, sprouts and seeded vegetables. Infection can cause fever, cramps and diarrhea.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

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

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameAbbott Laboratories
Recalling firmAbbott LaboratoriesAbbott Park, IL, United States
UPC / barcodes
0 70074 53511 10 70074 11629 70 70074 11985 4
Lot / date codes
  • Batches: 22331Z200 23377Z200 23438Z200 23439Z200 25562Z200 25562Z220 25563Z200 25729Z200 25730Z200 26731Z200 27922Z200 27931Z200 28124Z200 28125Z200 28126Z200 30291Z200 30292Z200 30517Z200 30518Z200 31392Z200 31402Z200 32421Z200 32684Z200 33694Z200 33695Z200 34012Z200 34769Z200 34770Z200 34771Z200 34771Z210 35023Z200 35032Z200 36149Z200 36150Z200 36151Z200 22331Z202 22331Z201
Distribution area
Nationwide

US Nationwide. Worldwide.

United States

Quantity affected425750 cases
Recall initiationFDA report date: March 16, 2022
FDA recall numberF-0949-2022

Beyond the headline

The recall, in context

Abbott Laboratories initiated this supplements recall on February 17, 2022. The FDA enforcement report states: Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced. The FDA report lists distribution as: US Nationwide. Worldwide.

The FDA enforcement report describes the reason as: Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

Abbott Elecare Amino Acid-based Powder Infant Formula with Iron 14.1oz was made or distributed by Abbott Laboratories in Abbott Park, IL, United States. This page reflects FDA report F-0949-2022, dated March 16, 2022.

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, a bacteria commonly linked to poultry, eggs, sprouts and seeded vegetables. Infection can cause fever, cramps and 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 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

Salmonella

Symptoms to watch for

Diarrhea, fever, abdominal cramps, nausea and sometimes vomiting. Symptoms can be severe in young children, older adults and immunocompromised people.

When symptoms may appear

Usually 6 hours to 6 days after exposure; illness often lasts 4 to 7 days.

Higher-risk groups

Children under 5, adults over 65, pregnant people and anyone with a weakened immune system are more likely to develop severe illness.

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 Abbott Elecare Amino Acid-based Powder Infant Formula with Iron 14.1oz recall?

Abbott Laboratories recalled Abbott Elecare Amino Acid-based Powder Infant Formula with Iron 14.1oz in an FDA Class I enforcement action reported as F-0949-2022. Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had…

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. 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 Abbott Laboratories 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-0949-2022. 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.