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Similac Probiotic Tri-Blend - recalled due to serious adverse reactions in preterm infants
1 year ago •source accessdata.fda.gov
Recall notice
United States
FDA announced the recall of 226,650 packets (4,533 cartons) of Similac Probiotic Tri-Blend by Abbott Laboratories due to serious adverse reactions in preterm infants. This product was distributed in Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, and West Virginia.The recalled product is:
- Similac Probiotic Tri-Blend - 0.017oz (0.50g) packaged in foil packets. 50 foil packets per carton - 3 cartons per case. Lot No. 45002IP Product No. 67397 Best By 09/01/24.
This recall was initiated on 10/31/2023 and its status is ongoing. Do not consume, sell, or distribute the recalled product.
If your infant is experiencing symptoms after eating the product it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist seek medical attention.
Source: www.accessdata.fda.gov/scripts/ires/index.cfm
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