RecallHawk

Portable Power Banks and Wireless Charging Stands

Belkin International Inc., of El Segundo, California

Summary

CPSC recall: Portable Power Banks and Wireless Charging Stands. By Belkin International Inc., of El Segundo, California. Hazard: The lithium-ion battery in the power banks and charging stands can overheat, posing fire and burn hazards to consumers.. Remedy: Consumers should immediately stop using the recalled power banks and charging stands and contact Belkin to receive a full refund or store credit. Consumers should submit photos showing the front and back of the product with their recall submi

Details

Source

CPSC Consumer Product Recall

External ID

10484

Action Date

2025-11-13

Status

Recalled

Category

consumer_product

Product Description

This recall involves charging stands with model number MMA008 and power banks with model numbers BPB002 and PB0003. Mode

Context & Analysis

This is a unclassified recall.

This was one of 20 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Belkin International Inc., of El Segundo, California 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 (Belkin International Inc., of El Segundo, California) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Belkin International Inc., of El Segundo, California have FDA actions?

Belkin International Inc., of El Segundo, California 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 "10484" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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