Recall Of Certain Powdered Infant Formula Produced In Abbott Nutrition’s Facility In Sturgis, Michigan

The FDA announced on February 17, 2022 that it is investigating consumer complaints of Cronobacter sakazakii and Salmonella Newport infections. All of the cases are reported to have consumed powdered infant formula produced from Abbott Nutrition’s Sturgis, Michigan facility. As a result of the ongoing investigation, along with the U.S. Centers for Disease Control and Prevention and state and local partners, the FDA is alerting consumers to avoid purchasing or using certain powdered infant formula products produced at this facility. No Abbott liquid formulas, powder formulas, or nutrition products from other facilities are impacted by the recall.

FDA has initiated an onsite inspection at the facility. Findings to date include several positive Cronobacter results from environmental samples taken by FDA, and adverse inspectional observations by FDA investigators. A review of the firm’s internal records also indicate environmental contamination with Cronobacter sakazakii and the firm’s destruction of product due to the presence of Cronobacter.

Cronobacter sakazakii is commonly found in the environment and a variety of areas in the home. Cronobacter bacteria can cause severe, life-threatening infections (sepsis) or meningitis (an inflammation of the membranes that protect the brain and spine). Symptoms of sepsis and meningitis may include poor feeding, irritability, temperature changes, jaundice (yellow skin and whites of the eyes), grunting breaths, and abnormal movements. Cronobacter infection may also cause bowel damage and may spread through the blood to other parts of the body. It can cause fever, poor feeding, excessive crying or low energy as well as other serious symptoms.

Salmonella are a group of bacteria that can cause gastrointestinal illness and fever called salmonellosis. Most people with salmonellosis develop diarrhea, fever and abdominal cramps. More severe cases of salmonellosis may include a high fever, aches, headaches, lethargy, a rash, blood in the urine or stool, and in some cases, may become fatal.

The FDA is investigating complaints of four infant illnesses from three states. All four cases related to these complaints were hospitalized and Cronobacter may have contributed to a death in one case.

The FDA is advising consumers not to use Similac, Alimentum, or EleCare powdered infant formulas if:

  • the first two digits of the code are 22 through 37; and
  • the code on the container contains K8, SH or Z2; and
  • the expiration date is 4-1-2022 (APR 2022) or later.

Parents and caregivers of infants who have used these products, and are concerned about the health of their child, should contact their child’s health care provider. If your child is experiencing any of these symptoms, you should notify your child’s healthcare provider and seek medical care for your child immediately.

The FDA warns that parents and caregivers should never dilute infant formula and should not make or feed homemade infant formula to infants. If your regular formula is not available, contact your child’s healthcare provider for recommendations on changing feeding practices.

Source

If your child was given infant formula impacted by the infant formula recall and your child suffered harm, call us on our toll-free number– 800-295-3959–to find infant formula recall lawyers who may investigate your claim for you and represent you and your child in a injury claim, if appropriate.

Turn to us when you don’t know where to turn.

This entry was posted on Saturday, February 19th, 2022 at 8:48 am. Both comments and pings are currently closed.

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