RecallHawk

Universal Broadmoore brand Bellevue and Oaklynn model canopy bed frames

Samson International, of High Point, North Carolina

Summary

CPSC recall: Universal Broadmoore brand Bellevue and Oaklynn model canopy bed frames. By Samson International, of High Point, North Carolina. Hazard: The canopy beams of the bed frames can collapse primarily when the bed is moved, posing impact and injury hazards to consumers.. Remedy: Consumers should not move the recalled bed frames and contact Samson International immediately for a free repair and installation kit consisting of four metal brackets and mounting hardware..

Details

Source

CPSC Consumer Product Recall

External ID

10692

Action Date

2026-04-02

Status

Recalled

Category

consumer_product

Product Description

This recall involves Samson International canopy bed frames sold under the Universal Broadmoor brand name. There are two

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.

Samson International, of High Point, North Carolina 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 (Samson International, of High Point, North Carolina) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Samson International, of High Point, North Carolina have FDA actions?

Samson International, of High Point, North Carolina 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 "10692" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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