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Class I: serious health riskOngoing

Abbott Similac Advance Step-2 22 Recall

Abbott Similac Advance Step-2 22

Abbott Laboratories · Abbott Park, IL

Risk level
Class I
Reported by FDA
Mar 16, 2022
Recall ID
F-0925-2022
Check your lot numberHow we source this data

Summary

Abbott Laboratories recalled Abbott Similac Advance Step-2 22 starting Feb 17, 2022. The FDA classified it as Class I (serious health risk) and published enforcement report F-0925-2022 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 Advance Step-2 22.5oz. plastic jar. 6 jars per case. Abbott Similac Advance 34oz. can. 6 cans per case. Abbott Similac Pro-Advance 20.6oz. and 859g. plastic jar. 6 jars per case. Item numbers: 6499113 6698313 6818113 6818313 Retail UPCs: 055325000808 055325001645 055325002864 055325002888

Lot numbers, UPCs & expiration codes

Batches: 27887SH00 31497SH00 35006SH00 23411SH00 25587SH00 26774SH00 27993SH00 28087SH00 29186SH00 30315SH00 31465SH00 31496SH00 35996SH00 36120SH10 36295SH10 32642SH00 35058SH10 35058SH00 36348SH00 37297SH00

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-0925-2022
Classification
Class I
Status
Ongoing
Recall initiated
Feb 17, 2022
FDA report date
Mar 16, 2022
Quantity
103025 cases
Recall type
Voluntary: Firm initiated
Recalling firm
Abbott Laboratories

Original FDA data

Every field from FDA enforcement report F-0925-2022, 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: 27887SH00 31497SH00 35006SH00 23411SH00 25587SH00 26774SH00 27993SH00 28087SH00 29186SH00 30315SH00 31465SH00 31496SH00 35996SH00 36120SH10 36295SH10 32642SH00 35058SH10 35058SH00 36348SH00 37297SH00
Postal code
60064-3502
Report date
Mar 16, 2022
Product type
Food
Recall number
F-0925-2022
Classification
Class I
Recalling firm
Abbott Laboratories
Product quantity
103025 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 Advance Step-2 22.5oz. plastic jar. 6 jars per case. Abbott Similac Advance 34oz. can. 6 cans per case. Abbott Similac Pro-Advance 20.6oz. and 859g. plastic jar. 6 jars per case. Item numbers: 6499113 6698313 6818113 6818313 Retail UPCs: 055325000808 055325001645 055325002864 055325002888
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-0925-2022, published Mar 16, 2022. View the source record (openFDA) · FDA enforcement reports

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

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