HR Platform Frames
Summary
CPSC recall: HR Platform Frames. By American Furniture Warehouse, Mattress Firm and furniture and mattress stores nationwide from April 2020 through January 2021 for about $200.. Hazard: The HR platform frame can collapse, posing a crush hazard that can result in severe injury or death.. Remedy: Consumers should immediately stop using the recalled HR Platform Frames and contact Global Home Imports to receive a free repair kit with metal clips to strengthen the frame. Global Home Imports will shi
Details
Source
CPSC Consumer Product Recall
External ID
9017
Action Date
2021-03-17
Status
Recalled
Category
consumer_product
Product Description
This recall involves HR Platform bed frames sold under the Bed Tech brand with model numbers HR33, HR33XL, HR46, HR50, H
Context & Analysis
This is a unclassified recall.
This was one of 6 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 (American Furniture Warehouse, Mattress Firm and furniture and mattress stores nationwide from April 2020 through January 2021 for about $200.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does American Furniture Warehouse, Mattress Firm and furniture and mattress stores nationwide from April 2020 through January 2021 for about $200. have FDA actions?
This is the only FDA action we have on record for American Furniture Warehouse, Mattress Firm and furniture and mattress stores nationwide from April 2020 through January 2021 for about $200. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9017" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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