CLASS I ONGOING Food recall · Reported 16 Mar 2022 · FDA Enforcement Report
Abbott Similac Pro-Advance, and.. can recalled by Abbott Laboratories
Abbott Laboratories is recalling Abbott Similac Pro-Advance, and.. can, distributed nationwide in the US. The recall was initiated on 17 Feb 2022 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0933-2022
- FDA event ID
- 89629
- Recalling firm
- Abbott Laboratories, Abbott Park, IL
- Brand
- Abbott Similac
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 17 Feb 2022
- FDA classified
- 30 Mar 2022
- Reported
- 16 Mar 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Salmonella
- Product category
- Baby Formula
Timeline
| 17 Feb 2022 | Recall initiated by company | |
| 16 Mar 2022 | Published in enforcement report | +27 days |
| 30 Mar 2022 | Classified by FDA | +14 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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
Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.
Product as listed by the FDA
Abbott Similac Pro-Advance 20.6oz., 30.3oz., 34oz., and 658g plastic jar. 6 jars per case. 7oz. can. 6 cans per case. Item numbers: 6720113 6720813 6726613 6818013 6818213 6832313 Retail UPCs: 055325002499 055325002543 055325002604 055325002819 055325002833 055325003069
Where it was distributed
US Nationwide. Worldwide.
Questions about this recall
Is Abbott Similac Pro-Advance, and.. can recalled?
Yes. Abbott Laboratories recalled Abbott Similac Pro-Advance, and.. can on 17 Feb 2022. The recall is Class I and its status is Ongoing. Recall number F-0933-2022.
Why was it 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
Which lots are affected?
Batches: 32624SH00 34958SH00 25673SH00 31463SH00 31549SH00 32625SH00 32626SH00 25604K800 31454K800 35008K800 37251K800 35055SH00 35056SH00 32624SH01 32625SH01 32626SH01
Where was it sold?
US Nationwide. Worldwide.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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