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A new tragic report has emerged of an infant fatality associated with cronobacter sakazakii bacteria, prompting Abbott to broaden its recall of powdered infant formulas. As of Tuesday, February 28, the FDA confirmed that one more infant death has been linked to formula produced at Abbott’s Sturgis, Michigan facility, bringing the total to five hospitalizations and two fatalities. Four of the affected infants were diagnosed with cronobacter sakazakii, while one was infected with salmonella. The cases have been reported across three states: Minnesota, Ohio, and Texas.
The latest death is connected to Similac 60/40, a specialty formula that was not part of the initial recall announced on February 17. This formula has been distributed in the U.S. and Israel and is now included in the recall.
The recall from February 17 includes powdered Similac, Alimentum, and Elecare infant formulas. It’s important to note that liquid formulas are not affected by this recall. The affected powdered formulas share these characteristics:
- The first two digits of the code are between 22-37;
- The code contains K8, SH, or Z2;
- The expiration date is April 1, 2022, or later.
Additionally, as of February 28, Similac 60/40 formula with lot codes 27032K80 (can) and 27032K800 (case) is now being recalled.
The FDA has stressed the importance of not diluting or creating homemade infant formula, emphasizing the safety of infants. Parents with affected products can either dispose of them or return them for a refund. Families receiving formula through WIC should take it back to the store for an exchange or refund.
During its investigation at Abbott’s Sturgis facility, the FDA found cronobacter sakazakii in environmental samples and noted several concerning inspection findings. Their review of Abbott’s internal documents also revealed contamination issues, with Abbott admitting to destroying contaminated formula.
While Abbott claims its internal testing has not detected cronobacter in the formula itself, they did find bacteria in non-product contact areas. Frank Yiannas, Deputy Commissioner for Food Policy and Response at the FDA, expressed deep concern over these reports, highlighting the serious risks associated with cronobacter, which can lead to life-threatening conditions like sepsis and meningitis in infants.
Symptoms of these infections can include poor feeding, irritability, fever, jaundice, grunting breaths, and abnormal movements, particularly in premature or immunocompromised infants. Salmonella infections can cause fever and diarrhea, with severe cases potentially leading to lethargy, rashes, and blood in urine or stool. Parents noticing these symptoms in their babies should consult a pediatrician immediately.
For more information on the recall, visit similacrecall.com.
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In summary, the recent expansion of Abbott’s infant formula recall has raised significant concerns regarding infant safety, particularly related to infections caused by cronobacter sakazakii and salmonella. Parents are urged to check their products and consult healthcare professionals if they notice any concerning symptoms in their infants.