CLASS I ONGOING Food recall · Reported 16 Mar 2022 · FDA Enforcement Report
Abbott EleCare Similac Gold recalled by Abbott Laboratories
Abbott Laboratories is recalling Abbott EleCare Similac Gold, 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-0929-2022
- FDA event ID
- 89629
- Recalling firm
- Abbott Laboratories, Abbott Park, IL
- Brand
- Abbott EleCare
- 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 EleCare HMO, Abbott Similac EleCare, Abbott EleCare Similac Gold, Abbott EleCare Similac 400g can. 6 cans per case Item numbers: 6676006 6676012 6676021 6676025 6676030 6676045 6676053 6676057 Retail UPCs: 8699548995217 0070074124155 0070074123851 0070074120195 070074120850 070074122502 0070074120157
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: 25557Z200 27930Z200 28130Z201 29266Z200 30374Z200 30384Z201 32422Z201 33693Z200 36144Z202 25557Z201 30384Z202 33693Z202 34767Z201 35031Z202 36144Z205 27930Z202 36144Z203 25557Z203 30374Z202 36144Z204 34767Z202 25557Z205 28130Z200 29266Z201 30384Z200 32422Z202 33693Z201 35031Z201 36144Z200 25557Z204 28130Z202 30374Z201 32422Z210 34767Z200 35031Z200 36144Z201 25557Z202 27930Z201 28130Z203
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.
More recalls from Abbott Laboratories
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|---|---|---|---|---|---|
| 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 |