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Class I: serious health riskOngoing

Abbott EleCare Recall

Abbott EleCare, EleCare LCP Hypoallergenic, Similac EleCare 400g

Abbott Laboratories · Abbott Park, IL

Risk level
Class I
Reported by FDA
Mar 16, 2022
Recall ID
F-0948-2022
Check your lot numberHow we source this data

Summary

Abbott Laboratories recalled Abbott EleCare starting Feb 17, 2022. The FDA classified it as Class I (serious health risk) and published enforcement report F-0948-2022 on Mar 16, 2022. Reason: 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. Status: Ongoing.

Why it was recalled

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

Product description

Abbott EleCare, EleCare LCP Hypoallergenic, Similac EleCare 400g. can. 6 cans per case. Item numbers: 5351034 5351066 5351039 5351077 Retail UPCs: 17703186031461 9340104000706 17501033957748 070074119281

Lot numbers, UPCs & expiration codes

Batches: 24549Z200 32429Z201 35025Z201 27871Z202 32429Z202 35025Z202 27871Z200 27871Z203 29258Z200 32429Z200 35025Z200 24549Z201 27871Z201 29258Z201 32429Z203

Where it was sold

US Nationwide. Worldwide.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0948-2022
Classification
Class I
Status
Ongoing
Recall initiated
Feb 17, 2022
FDA report date
Mar 16, 2022
Quantity
34585 cases
Recall type
Voluntary: Firm initiated
Recalling firm
Abbott Laboratories

Original FDA data

Every field from FDA enforcement report F-0948-2022, exactly as published.

Show all FDA fields
City
Abbott Park
State
IL
Status
Ongoing
Country
United States
Event ID
89629
Address
100 Abbott Park Rd Bldg Ap8b
Code information
Batches: 24549Z200 32429Z201 35025Z201 27871Z202 32429Z202 35025Z202 27871Z200 27871Z203 29258Z200 32429Z200 35025Z200 24549Z201 27871Z201 29258Z201 32429Z203
Postal code
60064-3502
Report date
Mar 16, 2022
Product type
Food
Recall number
F-0948-2022
Classification
Class I
Recalling firm
Abbott Laboratories
Product quantity
34585 cases
Reason for recall
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
Voluntary / mandated
Voluntary: Firm initiated
Product description
Abbott EleCare, EleCare LCP Hypoallergenic, Similac EleCare 400g. can. 6 cans per case. Item numbers: 5351034 5351066 5351039 5351077 Retail UPCs: 17703186031461 9340104000706 17501033957748 070074119281
Distribution pattern
US Nationwide. Worldwide.
Recall initiation date
Feb 17, 2022
Initial firm notification
Press Release
Center classification date
Mar 30, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0948-2022, published Mar 16, 2022. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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