RecallHawk
Class III Recall

Kroger 70% Isopropyl Alcohol, NET WT 5.5 OZ (156 g) per can, Distributed By The KROGER CO., Cincinnati, Ohio 45202. NDC

Consumer Product Partners, LLC

Summary

The FDA issued a Class III for Kroger 70% Isopropyl Alcohol, NET WT 5.5 OZ (156 g) per can, Distributed By The by Consumer Product Partners, LLC. Reason: Cross Contamination with Other Products..

Details

Source

Drug Recall

External ID

D-0660-2025

Action Date

2025-10-01

Status

Ongoing

Category

drug

Product Description

Kroger 70% Isopropyl Alcohol, NET WT 5.5 OZ (156 g) per can, Distributed By The KROGER CO., Cincinnati, Ohio 45202. NDC: 30142-810-14

Lot/Code Info: Lot 0662036; Exp. Date 06/19/2027

Quantity Affected: 1860 bottles

Reason for Recall

Cross Contamination with Other Products.

Distribution

US Nationwide.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-08-25

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 70 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.

Consumer Product Partners, LLC has 5 FDA actions in our database, including 5 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Consumer Product Partners, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Consumer Product Partners, LLC have FDA actions?

Consumer Product Partners, LLC has 5 FDA actions in our database, including 5 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0660-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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