DR Power LiPRO rechargeable lithium-ion battery packs (5.0 Ah)
Summary
CPSC recall: DR Power LiPRO rechargeable lithium-ion battery packs (5.0 Ah). By Ningbo New Team Import & Export Co. Ltd. ("Lera"), of China. Hazard: The recalled battery packs can short-circuit and ignite, posing fire and burn hazards to consumers.. Remedy: Consumers should immediately stop using the recalled battery packs and contact DR Power for a pro-rated refund, based on the battery's age. Consumers will need to show proof of the battery pack's destruction by uploading two photographs in ac
Details
Source
CPSC Consumer Product Recall
External ID
10321
Action Date
2025-06-26
Status
Recalled
Category
consumer_product
Product Description
This recall involves 62-volt 5.0 Ah LiPRO rechargeable lithium-ion battery packs for use with DR Power brand battery-pow
Context & Analysis
This is a unclassified recall.
This was one of 10 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Ningbo New Team Import & Export Co. Ltd. ("Lera"), 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 (Ningbo New Team Import & Export Co. Ltd. ("Lera"), 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 Ningbo New Team Import & Export Co. Ltd. ("Lera"), of China have FDA actions?
Ningbo New Team Import & Export Co. Ltd. ("Lera"), 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 "10321" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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