F-0956-2022 Class I Ongoing

Recalled by Abbott Laboratories — Abbott Park, IL

FDA food recall F-0956-2022 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: 40943 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
40943 cases

Product Description

Abbott Similac Alimentum Eye Q Plus 400g. can. Abbott Alimentum Eye Q 400g. can. Abbott Alimentum Eye Q Hypoallergenic 400g. can. 6 cans per case. Item numbers: 6208407 6208418 6208481 6208482 6208483 Retail UPCs: 070074110431 070074123905 070074110356 070074111834 070074110271

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: 26812Z261 29209Z201 30285Z263 32412Z222 33690Z201 26812Z262 27939Z263 29209Z203 30285Z262 32412Z223 26812Z263 27939Z260 29209Z200 30285Z260 32412Z220 32648Z200 26812Z260 27939Z261 29209Z202 30285Z261 32412Z221 33690Z200 33690Z210 27939Z262 29209Z204 30285Z264 32412Z224 33690Z202

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for F-0956-2022
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.