Zipadee Kids Convertible House Bed Frames and Montessori Floor Beds
Bell Station Interiors, dba Zipadee Kids, of Circleville, Ohio
Summary
CPSC recall: Zipadee Kids Convertible House Bed Frames and Montessori Floor Beds. By Bell Station Interiors, dba Zipadee Kids, of Circleville, Ohio. Hazard: The spindles used on the recalled beds are spaced at a distance that creates a serious entrapment hazard that can lead to strangulation and/or death to children. The design of the bed allows a child's torso to slip through the rail opening but will not allow their head to pass, posing entrapment and strangulation hazards that could result in
Details
Source
CPSC Consumer Product Recall
External ID
9690
Action Date
2023-08-17
Status
Recalled
Category
consumer_product
Product Description
This recall involves Zipadee Montessori beds sold in twin, full, and queen size variations of the "Convertible House Bed
Context & Analysis
This is a unclassified recall.
This was one of 13 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Bell Station Interiors, dba Zipadee Kids, of Circleville, Ohio 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 (Bell Station Interiors, dba Zipadee Kids, of Circleville, Ohio) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Bell Station Interiors, dba Zipadee Kids, of Circleville, Ohio have FDA actions?
Bell Station Interiors, dba Zipadee Kids, of Circleville, Ohio 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 "9690" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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