KingPavonini Adult Portable Bed Rails
Wuyi Fortune Land Sports and Leisure Products Co. Ltd., of China
Summary
CPSC recall: KingPavonini Adult Portable Bed Rails. By Wuyi Fortune Land Sports and Leisure Products Co. Ltd., of China. Hazard: The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning
Details
Source
CPSC Consumer Product Recall
External ID
10497
Action Date
2025-11-26
Status
Recalled
Category
consumer_product
Product Description
This recall involves six KingPavonini-branded adult portable bed rails with model numbers: BC-CBJ-X, BC-CBJ, BC-LDFS-X,
Context & Analysis
This is a unclassified recall.
This was one of 20 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Wuyi Fortune Land Sports and Leisure Products Co. Ltd., of China 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 (Wuyi Fortune Land Sports and Leisure Products Co. Ltd., of China) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Wuyi Fortune Land Sports and Leisure Products Co. Ltd., of China have FDA actions?
Wuyi Fortune Land Sports and Leisure Products Co. Ltd., of China 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 "10497" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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