Room & Board Griffin Duo Bunk Beds
Summary
CPSC recall: Room & Board Griffin Duo Bunk Beds. By Room & Board stores nationwide and online atwww.roomandboard.com from May 2013 through May 2017 for between $2,000 and $2,200.. Hazard: Some Griffin Duo Bunk Beds failed to be properly assembled by Room & Board with set screws installed into the side rail brackets at the time of delivery. Brackets lacking set screws can create a collapse risk, and fall and injury hazards.. Remedy: Consumers should immediately stop using the recalled bunk beds a
Details
Source
CPSC Consumer Product Recall
External ID
9800
Action Date
2023-12-14
Status
Recalled
Category
consumer_product
Product Description
This recall involves Room & Board's Griffin Duo Bunk Beds. The bunk beds are made from cherry wood or maple wood and hav
Context & Analysis
This is a unclassified recall.
This was one of 24 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 (Room & Board stores nationwide and online atwww.roomandboard.com from May 2013 through May 2017 for between $2,000 and $2,200.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Room & Board stores nationwide and online atwww.roomandboard.com from May 2013 through May 2017 for between $2,000 and $2,200. have FDA actions?
This is the only FDA action we have on record for Room & Board stores nationwide and online atwww.roomandboard.com from May 2013 through May 2017 for between $2,000 and $2,200. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9800" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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