RecallHawk

Aiper Elite Pro GS100 cordless robotic pool vacuum cleaners

Compurobot Technology Company, of China

Summary

CPSC recall: Aiper Elite Pro GS100 cordless robotic pool vacuum cleaners. By Compurobot Technology Company, of China. Hazard: When the charging cord is plugged into the device without the adapter and/or directly into the charging port on the machine, the battery can overheat and short circuit, posing burn and fire hazards.. Remedy: Consumers should immediately stop using the recalled pool vacuums and contact Aiper to receive a free replacement of Aiper's Seagull Pro robotic pool cleaner. Aiper w

Details

Source

CPSC Consumer Product Recall

External ID

9694

Action Date

2023-08-24

Status

Recalled

Category

consumer_product

Product Description

This recall involves Aiper Elite Pro cordless robotic pool vacuum cleaners with model number GS100. The Elite Pro unit w

Context & Analysis

This is a unclassified recall.

This was one of 6 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Compurobot Technology Company, 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 (Compurobot Technology Company, 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 Compurobot Technology Company, of China have FDA actions?

Compurobot Technology Company, 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 "9694" 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