RecallHawk

Aiper Seagull Pro ZT6001 cordless robotic pool cleaners

Dongguan Yuanhong Intelligent Technology Co. Ltd., of China

Summary

CPSC recall: Aiper Seagull Pro ZT6001 cordless robotic pool cleaners. By Dongguan Yuanhong Intelligent Technology Co. Ltd., of China. Hazard: The recalled pool vacuum cleaner has a large current adapter that can overheat, posing burn and fire hazards.. Remedy: Consumers should immediately stop using the recalled pool vacuums and contact Aiper to receive a free replacement Aiper Scuba S1 robotic pool cleaner. Aiper will provide a free return label for consumers to send the recalled product back t

Details

Source

CPSC Consumer Product Recall

External ID

10205

Action Date

2025-03-20

Status

Recalled

Category

consumer_product

Product Description

This recall involves Aiper Seagull Pro cordless robotic pool cleaners with model number ZT6001. The recalled pool vacuum

Context & Analysis

This is a unclassified recall.

This was one of 18 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Dongguan Yuanhong Intelligent Technology 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 (Dongguan Yuanhong Intelligent Technology 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 Dongguan Yuanhong Intelligent Technology Co. Ltd., of China have FDA actions?

Dongguan Yuanhong Intelligent Technology 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 "10205" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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