LUXE+WILLOW Heated Blankets
Summary
CPSC recall: LUXE+WILLOW Heated Blankets. By T.J. Maxx, Urban Outfitters and other stores nationwide from January 2022 through March 2022 for about $40.. Hazard: The blanket can overheat if left plugged in and powered on for an extended period of time, posing fire and burn hazards.. Remedy: Consumers should immediately stop using the recalled electric blanket and contact MWA for a full refund or $50 voucher towards the purchase of another LUXE+WILLOW product. Consumers should unplug the electric
Details
Source
CPSC Consumer Product Recall
External ID
9287
Action Date
2022-04-21
Status
Recalled
Category
consumer_product
Product Description
This recall involves LUXE+WILLOW Heated Blankets brand name L & W BIO. LUXE+WILLOW and L&W BIO are printed on a label on
Context & Analysis
This is a unclassified recall.
This was one of 14 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 (T.J. Maxx, Urban Outfitters and other stores nationwide from January 2022 through March 2022 for about $40.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does T.J. Maxx, Urban Outfitters and other stores nationwide from January 2022 through March 2022 for about $40. have FDA actions?
This is the only FDA action we have on record for T.J. Maxx, Urban Outfitters and other stores nationwide from January 2022 through March 2022 for about $40. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9287" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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