Powdered Infant Formula Recall: What You Need to Know

Powdered infant formula should be avoided if you are using Similac, Alimentum, and EleCare products.

U.S. Food and Drug Administration (FDA), is investigating complaints from consumers about bacterial infections in four infants who ingested powdered infant formula made at Abbott Nutrition’s Sturgis, Michigan facility. The bacterial infection could have caused death in two of the infants.

The FDA has published a complete list of Abbott Recalled Infant Formula brands. The FDA has withdrawn all recall products from sale. If you still have the products, make sure to check the lot code at the bottom of the package.

Parents and caregivers of infants who receive medical specialty infant formula or individuals who use certain medical foods will also find additional information from the FDA.

The FDA is aware of the concerns that parents and caregivers might have about infant formula as it is the only nutrition source for infants and newborns.

As we continue our investigation, here are some resources to assist you.

Recall of powdered infant formula products

Abbott Nutrition has recalled powdered infant formula products made at its Sturgis facility in Michigan. Some products from this facility were exported to countries and can be found all over the United States. Here are some ways to tell if you own any of these products.

The FDA advises that consumers examine the lot code on Similac, Alimentum, and EleCare powdered infant formulations. Do not use it if:

The codes’ first two digits are 22 to 37.

The code on the container has K8, SH, or Z2;

The expiration date is 4-1-2022, APR 2022 or later.

Abbott Nutrition has also recalled Similac 60/40, with a lot code 27032K80/27032K800 (case)

To verify if your product is included in the recall, you can also enter the lot code of your product on the company’s websiteExternal link Disclaimer For more information, please see the images below.

Recalls of powdered Abbott products without the expiration code and code noted above will not apply to these products. The recall does not apply to liquid formula products. Similac PM 60/40, lot code 27032K80 / 27032K800 / case are the only types and lots being recalled.

What was the exact date and location of the illnesses?

Between September 6, 2021, 2022, and January 4, 2022, there were a number of illnesses in Minnesota, Ohio and Texas.

I have difficulty finding the right formula. What can the FDA do to help me?

We are aware that the recall raised concerns about the availability and quality of certain infant formulas, especially given the strains experienced by supply chains during the COVID-19 pandemic.

The FDA continues to take significant steps to increase the supply of infant formula in America. Other infant formula manufacturers are exceeding or meeting current demand.

Abbott Nutrition is currently working with the FDA to assess the impact of the recall and determine the production capacity of other Abbott facilities that make some of the impacted brands. We are also working closely with Abbott to ensure safe resumption at the Sturgis facility in Michigan. The FDA reached out to other infant formula manufacturers as Abbott Nutrition initiated its Abbott Recalled Infant Formula. We will continue to talk with Abbott Nutrition, as well as other infant formula manufacturers, and we will consider all options for supporting the supply of infant formula products.

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