The Blue Cactus Company 2500 mAh Battery Packs for Reclining Chairs
Summary
CPSC recalled The Blue Cactus Company 2500 mAh Battery Packs for Reclining Chairs by Unknown Manufacturer. Hazard: The lithium-ion battery in the recalled battery packs can overheat, posing fire and burn hazards to consumers.. Remedy: Consumers should stop using the recalled battery packs immediately and contact The Blue Cactus Company for a replacement battery pack..
Details
Source
cpsc
External ID
26791
Action Date
2026-09-24
Status
Ongoing
Category
product
Product Code
Adapter/Power Supply/Charger/Battery
Product Description
This recall involves The Blue Cactus Company Reclining Chair 2500 mAh battery packs with model number RWX-RBP02. The battery packs are black with the brand logo and brand name of “The Blue Cactus Company” imprinted on the front. The recalled battery packs can be identified by the model number RWX-RBP02 printed on the rear of the product and were designed to be used with various brands of reclining chairs. Note: Do not throw this recalled lithium-ion battery or device in the trash, the general recycling stream (e.g., street-level or curbside recycling bins), or in used battery recycling boxes found at various retail and home improvement stores. Recalled lithium-ion batteries must be disposed of differently than other batteries, because they present a greater risk of fire. Your municipal household hazardous waste (HHW) collection center may accept this recalled lithium-ion battery or device for disposal. Before taking your battery or device to a HHW collection center, contact it ahead of time and ask whether it accepts recalled lithium-ion batteries. If it does not, contact your municipality for further guidance.
Company
Context & Analysis
Unknown Manufacturer has 1442 FDA actions in our database.
Frequently Asked Questions
How often does Unknown Manufacturer have FDA actions?
Unknown Manufacturer has 1442 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
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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