Food Recall Check
Class I · High risk Ongoing Initiated Feb 17, 2022 (5 years ago)

Abbott Similac Alimentum Eye Q Plus recall

Recalled by Abbott Laboratories · Abbott Park, IL, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was 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

Pathogen: Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

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

Quantity: 40943 cases

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

Nationwide.

FDA's distribution note: US Nationwide. Worldwide.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall.

Recalling firm
Abbott Laboratories
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 17, 2022
In FDA report of
Mar 16, 2022
FDA recall number
F-0956-2022 · event 89629
Official record
FDA enforcement report search

Also recalled with it (40 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class I · High risk Ongoing Salmonella

Abbott EleCare Infant Formula Unflavoured

Reason 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

Abbott Laboratories Nationwide F-0918-2022
Class I · High risk Ongoing Salmonella

Abbott Similac Human Milk Fortifier

Reason 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

Abbott Laboratories Nationwide F-0919-2022
Class I · High risk Ongoing Salmonella

Abbott Similac Alimentum Toddler Drink

Reason 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

Abbott Laboratories Nationwide F-0920-2022
Class I · High risk Ongoing Salmonella

Abbott Similac Total Comfort

Reason 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

Abbott Laboratories Nationwide F-0921-2022
Class I · High risk Ongoing Salmonella

Abbott Similac for Supplementation

Reason 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

Abbott Laboratories Nationwide F-0922-2022
Class I · High risk Ongoing Salmonella

Abbott Similac For Spit Up Infant Formula with Iron

Reason 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

Abbott Laboratories Nationwide F-0923-2022
Class I · High risk Ongoing Salmonella

Abbott Similac Advance Step-1

Reason 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

Abbott Laboratories Nationwide F-0924-2022
Class I · High risk Ongoing Salmonella

Abbott Similac Advance Step-2

Reason 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

Abbott Laboratories Nationwide F-0925-2022
Class I · High risk Ongoing Salmonella

Abbott Similac Sensitive Lactose Sensitivity

Reason 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

Abbott Laboratories Nationwide F-0926-2022
Class I · High risk Ongoing Salmonella

Abbott Similac Alimentum Infant Formula with Iron

Reason 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

Abbott Laboratories Nationwide F-0927-2022
Class I · High risk Ongoing Salmonella

Abbott Similac Total Comfort

Reason 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

Abbott Laboratories Nationwide F-0928-2022
Class I · High risk Ongoing Salmonella

Abbott Similac EleCare HMO

Reason 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

Abbott Laboratories Nationwide F-0929-2022

Showing 12 of 40.

Other recalls by Abbott Laboratories

Class II · Moderate risk Terminated Other

Similac Probiotic Tri-Blend

Reason Marketed towards preterm infants without approval as a new drug or licensed biologic, as well as unsafe food additive

Abbott Laboratories 41 states F-0328-2024