F-0155-2023 Class II Terminated

Recalled by Abbott Laboratories — Columbus, OH

FDA food recall F-0155-2023 was initiated by Abbott Laboratories on Oct 13, 2022 and is designated Class II. Reason for recall: Compromised seal integrity which could lead to spoilage The recall status is terminated (terminated Aug 14, 2024). Affected quantity: 14,588,544 bottles TOTAL.

Recall Details

Product Type
Food
Report Date
Nov 23, 2022
Initiation Date
Oct 13, 2022
Termination Date
Aug 14, 2024
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
14,588,544 bottles TOTAL

Product Description

Pedialyte Unflavored (Export to Canada) 2 fl oz plastic reclosable bottle 48 count case

Reason for Recall

Compromised seal integrity which could lead to spoilage

Distribution Pattern

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

Code Information

Batch No. 34589N200 Case No. 34589N200 Product No. 5989213 Best By 04/01/23

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for F-0155-2023
openFDA file date
Oct 23, 2026
Loaded by RegDataLab
Oct 23, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.