RecallHawk
Class I Recall

Abbott Similac Alimentum Eye Q Plus 400g. can. Abbott Alimentum Eye Q 400g. can. Abbott Alimentum Eye Q Hypoallergenic 4

Abbott Laboratories

Summary

The FDA issued a Class I for Abbott Similac Alimentum Eye Q Plus 400g. can. Abbott Alimentum Eye Q 400g. can. by Abbott Laboratories. Reason: Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facil.

Details

Source

Food Recall

External ID

F-0956-2022

Action Date

2022-03-16

Status

Ongoing

Category

food

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

Lot/Code Info: 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

Quantity Affected: 40943 cases

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

US Nationwide. Worldwide.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-02-17

Company

Abbott Laboratories

Abbott Park, IL

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 92 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Abbott Laboratories has 101 FDA actions in our database, including 86 recalls and 15 clearances.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Abbott Laboratories) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Abbott Laboratories have FDA actions?

Abbott Laboratories has 101 FDA actions in our database, including 86 recalls and 15 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0956-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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