RecallHawk

Sublue Mix underwater scooters and replacement batteries (black batteries only)

Unknown Manufacturer

Summary

CPSC recalled Sublue Mix underwater scooters and replacement batteries (black batteries only) by Unknown Manufacturer. Hazard: The lithium-ion batteries can overheat and ignite, posing a fire hazard to consumers.. Remedy: Consumers should stop using the scooters with the recalled batteries immediately and contact Sublue for a free new generation battery replacement (gray battery). Sublue will provide a battery collection kit for the consumer to return the recalled battery and will provide the replacement battery upon return of the recalled battery. Note: Do not throw this recalled battery in the trash or in used battery recycling boxes found at various retail and home improvement stores. Recalled lithium-ion batteries should be disposed of in accordance with any local and state ordinances, following the procedures established by municipal recycling centers for damaged, defective, or recalled lithium batteries, because these potentially hazardous batteries must be handled differently than other batteries..

Details

Source

cpsc

External ID

25169

Action Date

2025-03-13

Status

Ongoing

Category

product

Product Description

This recall involves certain Sublue Mix underwater scooter lithium-ion batteries and replacement batteries. The scooters are used for gliding through water. The batteries covered by the recall are black only. The scooters were sold in arctic white, space blue and aqua blue. The scooters have "Sublue" printed on the top and "Whiteshark Mix Underwater Scooter" printed on the side. The battery compartment is located on the underside of the scooter.

Context & Analysis

Unknown Manufacturer has 1320 FDA actions in our database.

Frequently Asked Questions

How often does Unknown Manufacturer have FDA actions?

Unknown Manufacturer has 1320 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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