RecallHawk

Metalux Optimized High Bay (OHB) LED Light Fixtures

Cooper Lighting, LLC, of Peachtree City, Georgia

Summary

CPSC recall: Metalux Optimized High Bay (OHB) LED Light Fixtures. By Cooper Lighting, LLC, of Peachtree City, Georgia. Hazard: The LED's board can overheat or come into contact with the lens or nearby combustible materials, posing a fire hazard.. Remedy: Consumers should stop using the recalled light fixtures immediately and contact Cooper Lighting to schedule a free repair or replacement. Consumers will be asked to complete a form at www.content.cooperlighting.com/ohb-recall to register the lig

Details

Source

CPSC Consumer Product Recall

External ID

10848

Action Date

2026-07-02

Status

Recalled

Category

consumer_product

Product Description

This recall involves Metalux Optimized High Bay (OHB) LED light fixtures used indoors in commercial structures with high

Context & Analysis

This is a unclassified recall.

This was one of 22 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Cooper Lighting, LLC, of Peachtree City, Georgia has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

What is a FDA 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 (Cooper Lighting, LLC, of Peachtree City, Georgia) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Cooper Lighting, LLC, of Peachtree City, Georgia have FDA actions?

Cooper Lighting, LLC, of Peachtree City, Georgia has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10848" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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