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Similac Powdered Infant Formula Recall Expanded

Abbott recently initiated a proactive, voluntary recall of powder formulas, including Similac, Alimentum and EleCare manufactured in Sturgis, Mich., one of the company’s manufacturing facilities. See initial recall information HERE.

The recall was expanded this week to include a specialty formula for infants with certain dietary needs. Abbott Nutrition is now recalling one lot of Similac PM 60/40 in addition to select lots of Similac, Alimentum, and EleCare formulas manufactured in its Sturgis, Michigan, facility. The products are sold throughout the U.S.

The Georgia Department of Public Health is urging parents and caregivers of infants to check their powdered infant formula before using it.

The recall for Similac PM 60/40 includes lot numbers 27032K80 on cans and 27032K800 on cases.

No distributed product has tested positive for the presence of Cronobacter sakazakii. Additionally, recently tested retained product samples of Similac PM 60/40 Lot # 27032K80 (can) / Lot #27032K800 (case) were negative for Cronobacter.

From Abbott: Abbott is voluntarily recalling one lot of Similac PM 60/40 (Lot # 27032K80 (can) / Lot # 27032K800 (case)) manufactured in Sturgis, Michigan. This is in addition to lots of Similac®, Alimentum® and EleCare® powder formula that were voluntarily recalled on Feb. 17. The action comes after learning of the death of an infant who tested positive for Cronobacter sakazakii and who we were informed had consumed Similac PM 60/40 from this lot. This case is under investigation, and at this time the cause of the infant’s Cronobacter sakazakii infection has not been determined. We want to extend our heartfelt sympathies to the family.

Parents can also check Similac’s recall website or call 800-986-8540 and follow the instructions provided to find out if a formula they use is included in the recall. If a child’s regular formula is not available, parents should consult with their child’s healthcare provider for recommendations on changing feeding practices.

Georgia WIC participants may return, or exchange recalled formula to the place of purchase or contact their WIC clinic to exchange for replacement vouchers.

The U.S. Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) are investigating after five babies in three states (Minnesota, Ohio, Texas) became sick with bacterial infections after consuming the products. Four of the complaints concerned Cronobacter sakazakii infections and one complaint was Salmonella infection. All five illnesses resulted in hospitalization and Cronobacter may have contributed to death in two infants.

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