Class IOngoing in FDA datasetRecall initiated Feb 17, 2022

Abbott Similac Pro-Advance 23oz. and 34oz. plastic jar. 6 jars per case. Item numbers: 6720413…

Recalling firm: Abbott Laboratories

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…

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ProductAbbott Similac Pro-Advance 23oz. and 34oz. plastic jar. 6 jars per case. Item numbers: 6720413 6721313 Retail UPCs: 055325002567 055325002581
Package size23oz

FDA code information

Batches: 30343SH00 34959SH00 24494SH00 30343SH01 32594SH00 32594SH10 32594SH20 34799SH00 34959SH01

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Full FDA record and distribution details

Original product description

Abbott Similac Pro-Advance 23oz. and 34oz. plastic jar. 6 jars per case. Item numbers: 6720413 6721313 Retail UPCs: 055325002567 055325002581

Original FDA recall 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

Recall details

Recall number
F-0932-2022
Event ID
89629
FDA status
Ongoing
Initiated
Feb 17, 2022
Reported
Mar 16, 2022
Classified
Mar 30, 2022
Quantity
26035 cases
Location
Abbott Park, IL, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

US Nationwide. Worldwide.

FDA source record · F-0932-2022

Data updated September 16, 2026. View official FDA data ↗

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