A tragic update has emerged regarding the recall of powdered infant formula, as another infant has died after contracting the cronobacter sakazakii bacteria. The FDA announced on February 28 that this latest death is connected to formula produced by Abbott at its facility in Sturgis, Michigan. This brings the total number of reported hospitalizations to five, including two fatalities. Among these cases, four babies were infected with cronobacter sakazakii, while one was affected by salmonella. The illnesses have been reported across three states: Minnesota, Ohio, and Texas.
The most recent fatality is associated with Similac 60/40, a specialty formula that was not part of Abbott’s initial recall issued on February 17. This particular formula has now been added to the recall list and was distributed in both the U.S. and Israel. The February 17 recall specifically pertains to certain powdered Similac, Alimentum, and Elecare formulas, while liquid products remain unaffected. These formulas were distributed widely in the U.S. and potentially in other countries.
Recall Criteria
The initial recall criteria for the affected formulas include:
- The first two digits of the code range from 22-37;
- The container code includes K8, SH, or Z2;
- The expiration date is April 1, 2022, or later.
As of February 28, the recall now includes Similac 60/40 formula with lot codes 27032K80 (can) and 27032K800 (case). The FDA advises caregivers against diluting infant formula or using homemade alternatives. Consumers with affected products can either dispose of them or return them for a refund. Families receiving formula through WIC should return it to the store for exchange or refund.
During its investigation at Abbott’s facility, the FDA discovered positive results for cronobacter sakazakii in environmental samples, as well as adverse inspection findings. Abbott stated that its internal testing has not revealed evidence of cronobacter within its formula, although traces of the bacteria were found in non-product contact areas.
Frank Yiannas, FDA Deputy Commissioner for Food Policy and Response, expressed deep concern over these bacterial infection reports, given the critical nature of infant formula as a primary nutrition source for many newborns. Cronobacter can lead to severe infections such as sepsis or meningitis, which are particularly dangerous for premature or immunocompromised infants. Symptoms of these conditions can include poor feeding, irritability, fever, jaundice, and unusual movements. Salmonella infections typically present with fever and diarrhea but can also lead to more severe symptoms.
If your baby displays any of these concerning symptoms, it is essential to consult your pediatrician. Parents or customers with affected products can find more information at similacrecall.com.
For additional information on topics related to pregnancy and home insemination, we invite you to explore other resources like Progyny’s blog and Intracervical Insemination, both of which provide valuable insights.
Summary
Recent reports have linked the death of another infant to Abbott’s recalled powdered formula. The FDA has expanded the recall to include additional products, while investigations reveal contamination concerns at Abbott’s facility. Parents are urged to check their products and consult with healthcare providers if symptoms arise.