RecallHawk

Usines Giant Factories Gas Water Heaters with Emerson control valves

White-Rodgers, a division of Emerson Electric Co., Saint Louis, Missouri (control valve)

Summary

CPSC recall: Usines Giant Factories Gas Water Heaters with Emerson control valves. By White-Rodgers, a division of Emerson Electric Co., Saint Louis, Missouri (control valve). Hazard: The power handle can short circuit and overheat, posing fire and burn hazards. Remedy: Consumers should immediately contact Usines Giant Factories, who will arrange to have the Emerson control valve replaced by a certified technician, and to receive a free replacement valve. Consumers who continue to use the water

Details

Source

CPSC Consumer Product Recall

External ID

9167

Action Date

2021-11-03

Status

Recalled

Category

consumer_product

Product Description

The recall involves propane and natural gas water heaters in 40, 50, and 75 gallon capacities. The recalled water heater

Context & Analysis

This is a unclassified recall.

This was one of 8 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

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 (White-Rodgers, a division of Emerson Electric Co., Saint Louis, Missouri (control valve)) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does White-Rodgers, a division of Emerson Electric Co., Saint Louis, Missouri (control valve) have FDA actions?

This is the only FDA action we have on record for White-Rodgers, a division of Emerson Electric Co., Saint Louis, Missouri (control valve) in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9167" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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