Abbott Similac for Supplementation 22oz — Class I food recall F-0922-2022
Ongoing recall by Abbott Laboratories, reported 2022-03-16, distributed nationwide. Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobac
| Recall number | F-0922-2022 |
|---|---|
| Product type | Food |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Abbott Laboratories, Abbott Park, IL, United States |
| Recall initiated | 2022-02-17 |
| Classified | 2022-03-30 |
| Reported by FDA | 2022-03-16 |
| Distributed | Nationwide (US) |
| Quantity | 22,074 cases |
| Reason classes | microbial contamination |
| Pathogens | salmonella, cronobacter |
| UPC / GTIN / UDI-DI | 00070074629506 |
| Lot numbers | 24511SH00, 27083SH00 |
| Model numbers | 63013 |
Product
Abbott Similac for Supplementation 22oz. plastic jar. 4 jars per case. Item numbers: 63013 Retail UPCs: 070074629506 70074629506
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-0922-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.