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Help is on the way to combat baby formula shortages

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Photo courtesy of Abbott

ABBOTT PARK, Ill., May 16, 2022 /PRNewswire/ — Abbott has agreed to enter into a consent decree with the U.S. Food and Drug Administration (FDA) related to its Sturgis, Mich., infant formula plant. The decree is an agreement between FDA and Abbott on the steps necessary to resume production and maintain the facility. This does not affect any other Abbott plant or operation. The decree is subject to court approval.

“Our number one priority is getting infants and families the high-quality formulas they need, and this is a major step toward re-opening our Sturgis facility so we can ease the nationwide formula shortage. We look forward to working with the FDA to quickly and safely re-open the facility,” said Robert B. Ford, chairman and chief executive officer, Abbott. “We know millions of parents and caregivers depend on us and we’re deeply sorry that our voluntary recall worsened the nationwide formula shortage. We will work hard to re-earn the trust that moms, dads and caregivers have placed in our formulas for more than 50 years.”

Once the FDA confirms the initial requirements for start-up have been met, Abbott could restart the site within two weeks. The company would begin production of EleCare®, Alimentum® and metabolic formulas first and then begin production of Similac® and other formulas. From the time Abbott restarts the site, it will take six to eight weeks before product is available on shelves.

“Our safety and quality processes meet even the toughest scrutiny and we’re committed to continuously improving our processes and protocols,” said Mr. Ford. “Nutrition is fundamental to Abbott and to our goal of improving the lives of more than 3 billion people by decade’s end. We intend to set the standard for the industry, raising the bar on both safety and quality.”

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