Recall map → All recalls → F-0328-2024
Similac Probiotic Tri-Blend - 0.017oz (0.50g) packaged in foil packets. 50 foil packets per carton - 3 cartons per case. Abbott Laboratories · reported 2023-11-15
Terminated This recall has been closed out by the agency.
- Reason for recall
- Marketed towards preterm infants without approval as a new drug or licensed biologic, as well as unsafe food additive
- Classification
- Class II
- Recall initiated
- 2023-10-31
- Reported by the agency
- 2023-11-15
- Closed out (terminated)
- 2024-09-03
- Recalling firm
- Abbott Laboratories
Columbus, OH
United StatesThis is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.
- Distribution (the agency's own words)
- 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, West Virginia
- States we parsed from that text
- AL AR AZ CA CO CT FL GA IA ID IL IN KY LA MA MD ME MI MN MO MS MT NC ND NE NJ NM NV NY OH OK PA SC SD TN TX UT VA WA WI WV
The agency named these states. Parse method explicit_state_list, confidence high.
- Food category
- Dietary supplementsderived
Assigned by a reviewed keyword rulebook over the product description, not by the agency.
- Recall type
- Voluntary: Firm initiated
- Recall number
- F-0328-2024
View this record at the agency source →
This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.