RecallHawk

Square™ D QO™ Plug-on-Neutral Load Centers, also known as, Load Centers, Breaker Boxes, Electrical Panels

Schneider Electric USA Inc., of Lexington, Kentucky

Summary

CPSC recall: Square™ D QO™ Plug-on-Neutral Load Centers, also known as, Load Centers, Breaker Boxes, Electrical Panels. By Schneider Electric USA Inc., of Lexington, Kentucky. Hazard: The load center can overheat, posing thermal burn and fire hazards.. Remedy: Schneider Electric is directly contacting all known retailers, distributors, homeowners, and any other individuals that purchased or installed the recalled product. All purchasers and installers should immediately contact Schneider Electri

Details

Source

CPSC Consumer Product Recall

External ID

9325

Action Date

2022-06-16

Status

Recalled

Category

consumer_product

Product Description

This recall involves indoor, outdoor and original equipment manufacturer (OEM) Square D QO Plug-On Neutral Load Centers

Context & Analysis

This is a unclassified recall.

This was one of 17 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Schneider Electric USA Inc., of Lexington, Kentucky 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 (Schneider Electric USA Inc., of Lexington, Kentucky) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Schneider Electric USA Inc., of Lexington, Kentucky have FDA actions?

Schneider Electric USA Inc., of Lexington, Kentucky 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 "9325" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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