RecallHawk

Style Selections 42-inch-wide Infrared Quartz Electric Fireplaces

Twin-Star International Inc, of Boca Raton, Florida

Summary

CPSC recall: Style Selections 42-inch-wide Infrared Quartz Electric Fireplaces. By Twin-Star International Inc, of Boca Raton, Florida. Hazard: The electric fireplaces can overheat, posing a fire hazard.. Remedy: Consumers should immediately stop using and unplug the recalled electric fireplace and contact Twin-Star for a refund of the purchase price. Consumers should complete the online recall registration form at www.twinstarhome.com/recall or call Twin-Star for information on how to take part

Details

Source

CPSC Consumer Product Recall

External ID

9753

Action Date

2023-11-09

Status

Recalled

Category

consumer_product

Product Description

This recall involves Twin-Star Style Selections 42-inch-wide, 5,200 BTU, Black Infrared Quartz Electric Fireplace with m

Context & Analysis

This is a unclassified recall.

This was one of 15 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Twin-Star International Inc, of Boca Raton, Florida 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 (Twin-Star International Inc, of Boca Raton, Florida) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Twin-Star International Inc, of Boca Raton, Florida have FDA actions?

Twin-Star International Inc, of Boca Raton, Florida 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 "9753" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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