RecallHawk

Babyletto Kiwi Electronic Recliner and Swivel Gliders with USB port

Guangzhou Plenty Bicycle Co., Ltd., of China

Summary

CPSC recall: Babyletto Kiwi Electronic Recliner and Swivel Gliders with USB port. By Guangzhou Plenty Bicycle Co., Ltd., of China. Hazard: The USB module in the recliner arm can overheat and spark, posing an overheating hazard.. Remedy: Consumers should immediately stop using the recalled recliners and contact Babyletto to receive a free repair kit. Consumers should register at babylettorecall.com/ to receive their free repair kit and installation instructions. Once consumers have completed the

Details

Source

CPSC Consumer Product Recall

External ID

10349

Action Date

2025-07-17

Status

Recalled

Category

consumer_product

Product Description

This recall involves Babyletto Kiwi Electronic Recliner and Glider fabric-covered chairs with two USB device charging po

Context & Analysis

This is a unclassified recall.

This was one of 14 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Guangzhou Plenty Bicycle Co., Ltd., of China has 4 FDA actions in our database, including 2 recalls.

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 (Guangzhou Plenty Bicycle 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 Guangzhou Plenty Bicycle Co., Ltd., of China have FDA actions?

Guangzhou Plenty Bicycle Co., Ltd., of China has 4 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10349" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for consumer_product

Related Actions