CLASS I ONGOING Food recall · Reported 16 Mar 2022 · FDA Enforcement Report
Abbott Similac Total Comfort recalled by Abbott Laboratories
Abbott Laboratories is recalling Abbott Similac Total Comfort and can.. Abbott Similac Advance Step-2 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-0928-2022
- 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 Total Comfort 638g. plastic jar and 8oz. can. 6 units per case. Abbott Similac Advance Step-2 34oz. can. 6 cans per case. Item numbers: 6635013 6635113 6698413 Retail UPCs: 055325626602 055325626626 055325001652
Where it was distributed
US Nationwide. Worldwide.
Questions about this recall
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: 23420SH00 32608SH00 26820K800 33725K800 37277K800 26821SH00 28089SH00 29245SH00 32607SH00 34861SH00 36124SH00
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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
40 other products · FDA event 89629This product is part of a recall event; the main page for the event is Abbott Similac Advance Infant Formula recalled by Abbott Laboratories.
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Other Baby Formula recalls
All 76| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS I | a.) nara organics Whole Milk Organic Infant Formula recalled | Nara Organics | Botulism | Nationwide |
| Food | CLASS I | a2 Platinum Premium infant formula Milk-based Powder with Iron recalled | The a2 Milk | Foreign Material | Nationwide |
| Food | CLASS II | Valley Springs 100% Natural Bottled Water recalledValley Springs | Valley Springs Artesian Gold | Foreign Material | IL, WI |
| Food | CLASS I | ByHeart Whole Nutrition Infant Formula recalled | ByHeart | Botulism | Nationwide |
| Food | CLASS II | CVS Health and HEB Baby brand Premium Infant Formula recalledCVS Health | PBM Nutritionals | Packaging Defects | 12 states |