RecallHawk

EverFrost Battery Powered Coolers

Anker Innovations Limited, of Hong Kong

Summary

CPSC recalled EverFrost Battery Powered Coolers by Anker Innovations Limited, of Hong Kong. Hazard: The lithium-ion batteries in the Anker EverFrost Coolers can overheat, posing a fire hazard.. Remedy: Consumers should immediately stop using the recalled coolers, and contact Anker for a free replacement lithium-ion battery pack. Visit https://www.anker.com/anker-solix/cooler-battery-recall-pps to file a claim, and for instructions on how to replace the battery pack. Recalled lithium-ion batteries should be disposed of in accordance with any local and state laws, and not in the trash..

Details

Source

cpsc

External ID

24146

Action Date

2024-03-07

Status

Ongoing

Category

product

Product Description

This recall involves the lithium-ion battery packs in Anker EverFrost Coolers. The coolers are intended for use in outdoor camping, travel and fishing for cooling and freezing food or medicine. They are dark gray with wheels and a drop-down rolling handle. There is a blue charging port for charging by alternative power sources, such as plug-in or solar, on one end of the cooler. The name "Anker EverFrost" appears on the side in silver and blue. The model number is printed on the outer surface on the bottom of the cooler. The following model numbers are included in this recall: Product Model # Size Anker Detachable Battery pack for Powered Cooler A17B0 Not Applicable Anker EverFrost Powered Coolers 30 A17A0 33 Liter Anker EverFrost Powered Coolers 40 A17A1 43 Liters Anker EverFrost Powered Coolers 50 A17A2 53 Liters

Context & Analysis

Anker Innovations Limited, of Hong Kong has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

How often does Anker Innovations Limited, of Hong Kong have FDA actions?

Anker Innovations Limited, of Hong Kong 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. 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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