CLASS I ONGOING Food recall · Reported 16 Mar 2022 · FDA Enforcement Report
Abbott Similac Pro-Total Comfort Infant Formula recalled
Abbott Laboratories is recalling Abbott Similac Pro-Total Comfort Infant Formula with Iron 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-0934-2022
- 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-Total Comfort Infant Formula with Iron 20.1oz. and 22.5oz. plastic jar. 4 jars per case. 34oz. plastic jar. 6 jars per case. 7oz. can. 6 cans per case. Item numbers: 66798 66939 67925 68107 Retail UPCs: 070074667997 070074669403 070074679266 070074681085
Where it was distributed
US Nationwide. Worldwide.
Questions about this recall
Is Abbott Similac Pro-Total Comfort Infant Formula with Iron and.... can recalled?
Yes. Abbott Laboratories recalled Abbott Similac Pro-Total Comfort Infant Formula with Iron and.... can on 17 Feb 2022. The recall is Class I and its status is Ongoing. Recall number F-0934-2022.
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: 26838SH00 26860SH00 26861SH00 30318SH00 31498SH00 31580SH00 33730SH00 24451SH00 24565SH00 26738SH00 26791SH00 23495K800 24481K800 25572K800 25588K800 26739K800 26837K800 28014K800 28141K800 28152K800 29243K800 29246K800 30319K800 31466K800 31579K800 31581K800 32613K800 32614K800 34860K800 36123K800 37236K800 27977SH00 27978SH00 27990SH00 28096SH00 28097SH00 30303SH00 30304SH00 31582SH00 31583SH00 33726SH00 33727SH00 33728SH00 33729SH00 37237SH00 37303SH00
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.
More recalls from Abbott Laboratories
All 153| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Alinity hq Analyzer recalled by Abbott Laboratories | Abbott Laboratories | Device Malfunction | Nationwide |
| Device | CLASS II | Cell-dyn Ruby recalled by Abbott Laboratories | Abbott Laboratories | Device Malfunction | Nationwide |
| Device | CLASS II | Cell-dyn Ruby recalled by Abbott Laboratories | Abbott Laboratories | Device Malfunction | Nationwide |
| Device | CLASS II | Cell-dyn Ruby recalled by Abbott Laboratories | Abbott Laboratories | Device Malfunction | Nationwide |
| Device | CLASS II | Cell-dyn Ruby recalled by Abbott Laboratories | Abbott Laboratories | Device Malfunction | Nationwide |
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 |