RecallHawk

High Bay Linear LED light fixtures

Jiangsu Ever-Tie Lighting Co., Ltd, of China

Summary

CPSC recall: High Bay Linear LED light fixtures. By Jiangsu Ever-Tie Lighting Co., Ltd, of China. Hazard: The retaining pins used to secure the LED board inside some units can degrade, the LED board to come loose inside the fixture, posing a fire hazard.. Remedy: Consumers should immediately stop using the High Bay Linear LED light fixtures and contact PQL for free replacement retaining pins. Consumers should register their product at https://pqlighting.com/product-recall-notice..

Details

Source

CPSC Consumer Product Recall

External ID

10625

Action Date

2026-02-26

Status

Recalled

Category

consumer_product

Product Description

This recall involves High Bay Linear LED light fixtures. The fixtures are rectangular, white, metal, and are available i

Context & Analysis

This is a unclassified recall.

This was one of 35 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Jiangsu Ever-Tie Lighting Co., Ltd, of China 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 (Jiangsu Ever-Tie Lighting Co., Ltd, of China) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Jiangsu Ever-Tie Lighting Co., Ltd, of China have FDA actions?

Jiangsu Ever-Tie Lighting Co., Ltd, of China 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 "10625" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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