RecallHawk

Merax Full-Size and Twin-Size Murphy Beds

Unknown Manufacturer

Summary

CPSC recalled Merax Full-Size and Twin-Size Murphy Beds by Unknown Manufacturer. Hazard: During assembly or disassembly, the frame of the wall bed can fall onto consumers, posing deadly impact, crush and laceration hazards.. Remedy: Consumers should stop using the recalled Murphy beds immediately and contact GigaCloud Technology for a free repair kit. Consumers that have not assembled the Murphy bed will receive a repair kit consisting of unloaded piston springs, updated assembly instructions and inspection instructions. Consumers that have assembled the Murphy bed will receive inspection instructions. If the consumer determines that the Murphy bed is assembled incorrectly, GigaCloud Technology will provide the consumer with a professional installer to correct or complete the installation, at no cost to the consumer..

Details

Source

cpsc

External ID

26694

Action Date

2026-08-13

Status

Ongoing

Category

product

Product Description

This recall involves full-size and twin-size Merax Murphy beds with model numbers GX000392AAK, GX000391AAK or GX000383AAK, all sold in white. The beds are designed to be wall-mounted and can fold into a cabinet. The following model numbers and SKU codes are included in the recall: Model Number SKU Codes Dimensions GX000392AAK WF530245, WF530246, WF530247, WF530248 78.2" L x 108.4" W x 99" H GX000391AAK WF530240, WF530241, WF530242, WF530243 78.2" L x 93.2" W x 99" H GX000383AAK WF324470, WF324471, WF324472 76" L x 95.2" W x 83.8" H The same product may have been sold by other marketplace sellers under different brand names such as Euroco, Harper & Bright Designs, Modern Luxe, Polibi, other brand names or without a brand name. The SKU code on all recalled products, regardless of brand name, is located on a sticker on the inside frame of the recalled Murphy beds.

Context & Analysis

Unknown Manufacturer has 1380 FDA actions in our database.

Frequently Asked Questions

How often does Unknown Manufacturer have FDA actions?

Unknown Manufacturer has 1380 FDA actions in our database, including 0 recalls and 0 device clearances.

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The official record is available on FDA.gov. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.

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