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Class I: serious health riskOngoing

Abbott Similac for Supplementation 22oz Recall

Abbott Similac for Supplementation 22oz

Abbott Laboratories · Abbott Park, IL

Risk level
Class I
Reported by FDA
Mar 16, 2022
Recall ID
F-0922-2022
Check your lot numberHow we source this data

Summary

Abbott Laboratories recalled Abbott Similac for Supplementation 22oz starting Feb 17, 2022. The FDA classified it as Class I (serious health risk) and published enforcement report F-0922-2022 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 Similac for Supplementation 22oz. plastic jar. 4 jars per case. Item numbers: 63013 Retail UPCs: 070074629506 70074629506

Lot numbers, UPCs & expiration codes

Batches: 24511SH00 27083SH00

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-0922-2022
Classification
Class I
Status
Ongoing
Recall initiated
Feb 17, 2022
FDA report date
Mar 16, 2022
Quantity
22074 cases
Recall type
Voluntary: Firm initiated
Recalling firm
Abbott Laboratories

Original FDA data

Every field from FDA enforcement report F-0922-2022, 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: 24511SH00 27083SH00
Postal code
60064-3502
Report date
Mar 16, 2022
Product type
Food
Recall number
F-0922-2022
Classification
Class I
Recalling firm
Abbott Laboratories
Product quantity
22074 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 Similac for Supplementation 22oz. plastic jar. 4 jars per case. Item numbers: 63013 Retail UPCs: 070074629506 70074629506
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-0922-2022, published Mar 16, 2022. View the source record (openFDA) · FDA enforcement reports

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

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