F-0948-2022 Class I Ongoing

Recalled by Abbott Laboratories — Abbott Park, IL

FDA food recall F-0948-2022 was initiated by Abbott Laboratories on Feb 17, 2022 and is designated Class I. 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 The recall status is ongoing. Affected quantity: 34585 cases.

Recall Details

Product Type
Food
Report Date
Mar 16, 2022
Initiation Date
Feb 17, 2022
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
34585 cases

Product Description

Abbott EleCare, EleCare LCP Hypoallergenic, Similac EleCare 400g. can. 6 cans per case. Item numbers: 5351034 5351066 5351039 5351077 Retail UPCs: 17703186031461 9340104000706 17501033957748 070074119281

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

Distribution Pattern

US Nationwide. Worldwide.

Code Information

Batches: 24549Z200 32429Z201 35025Z201 27871Z202 32429Z202 35025Z202 27871Z200 27871Z203 29258Z200 32429Z200 35025Z200 24549Z201 27871Z201 29258Z201 32429Z203

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for F-0948-2022
openFDA file date
Oct 6, 2026
Loaded by RegDataLab
Oct 6, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it. FDA may have changed the recall since.