Class IITerminated in FDA datasetOct 13, 2022

Similac Water - Sterilized (Export Canada) 2 fl oz reclose able plastic bottle Packaged as: 48 count case

Recalling firm: Abbott Laboratories

Why it was recalled

Compromised seal integrity which could lead to spoilage

Check the codes ↓

The exact product

Similac Water - Sterilized (Export Canada) 2 fl oz reclose able plastic bottle Packaged as: 48 count case

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

Batch No. 39398N200 Case No. 39398N200 Product No. 5100013 Best By 10/01/23

TypeCode / valueContext
best by10/01/23Batch No. 39398N200 Case No. 39398N200 Product No. 5100013 Best By 10/01/23

Recall details

Recall number
F-0165-2023
Event ID
91003
FDA status
Terminated
Initiated
Oct 13, 2022
Reported
Nov 23, 2022
Classified
Nov 16, 2022
Terminated
Aug 14, 2024
Quantity
14,588,544 bottles TOTAL
Location
Columbus, OH, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Domestic: Alaska, Alabama, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maine, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Washington DC, Wisconsin, West Virginia, Wyoming Foreign: Canada, Puerto Rico, Bermuda, Curacao, Trinidad, Tobago, Panama, Dominican Republic, and Colombia

FDA source record · F-0165-2023

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.