# FDA recall F-0328-2024

> **Abbott Laboratories** · Class II · food recall initiated 2023-10-31.

## Product

Similac Probiotic Tri-Blend - 0.017oz (0.50g) packaged in foil packets. 50 foil packets per carton - 3 cartons per case.

## Reason for recall

Marketed towards preterm infants without approval as a new drug or licensed biologic, as well as unsafe food additive

## Distribution

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

## Key facts

- **Recall number:** F-0328-2024
- **Recalling firm:** Abbott Laboratories
- **Classification:** Class II
- **Product type:** food
- **Status:** Terminated
- **Initiation date:** 2023-10-31
- **Report date:** 2023-11-15
- **Termination date:** 2024-09-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Columbus, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-0328-2024

## Citation

> AI Analytics. FDA recall F-0328-2024. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/F-0328-2024. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*