Recall · openFDA Food Enforcement

Similac Probiotic Tri-Blend - 0.017oz (0.50g) packaged in foil…: FDA Recall F-0328-2024

Agency action: Oct 31, 2023Record ID: F-0328-2024
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What happened

Original notice title

Similac Probiotic Tri-Blend - 0.017oz (0.50g) packaged in foil packets. 50 foil packets per carton - 3 cartons per case., recall F-0328-2024

From the archived source record

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

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

Read the official notice →

Status and source details

Status recorded in the archive
Terminated
FDA recall classification
Class II
Recall initiated by
Voluntary: Firm initiated
Report date
Nov 15, 2023
Termination date in the archive
Sep 3, 2024
Source checked
Jul 16, 2026
Record revision
64da4ae54697

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

Sources, dates, and coverage →

What is affected

Product
Similac Probiotic Tri-Blend - 0.017oz (0.50g) packaged in foil packets. 50 foil packets per carton - 3 cartons per case.
Company
Abbott Laboratories
Lot / identifier
Lot No. 45002IP Product No. 67397 Best By 09/01/24
Market / 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