SRTH Small Room Tower Heaters
Summary
CPSC recall: SRTH Small Room Tower Heaters. By Bed Bath & Beyond and other stores nationwide and online at Amazon.com and other websites from November 2022 through December 2022 for about $50.. Hazard: The heaters have a miswiring due to a manufacturing error which can cause the tower heater to overheat, posing a fire hazard.. Remedy: Consumers should immediately stop using the recalled heaters and visit Vornado's website to register for the recall and to receive a full refund..
Details
Source
CPSC Consumer Product Recall
External ID
9558
Action Date
2023-03-09
Status
Recalled
Category
consumer_product
Product Description
This recall involves Vornado SRTH Small Room Tower Heaters with a "JUL22" date code and "TYPE SRTH" printed on the silve
Context & Analysis
This is a unclassified recall.
This was one of 19 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 (Bed Bath & Beyond and other stores nationwide and online at Amazon.com and other websites from November 2022 through December 2022 for about $50.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Bed Bath & Beyond and other stores nationwide and online at Amazon.com and other websites from November 2022 through December 2022 for about $50. have FDA actions?
This is the only FDA action we have on record for Bed Bath & Beyond and other stores nationwide and online at Amazon.com and other websites from November 2022 through December 2022 for about $50. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9558" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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