FENGQS F7 Pro E-bikes
Shenzhen Fengqisi Car Industry Co., Ltd., dba FENGQS, of China
Summary
CPSC recall: FENGQS F7 Pro E-bikes. By Shenzhen Fengqisi Car Industry Co., Ltd., dba FENGQS, of China. Hazard: The e-bikes' lithium-ion battery can overheat and ignite, posing serious fire and burn hazards to consumers.. Remedy: Consumers should stop using the recalled e-bikes immediately and contact FENGQS for a full refund. Consumers will be asked to write their name, the word "recalled," and the current date next to the battery's production date, with a permanent marker. Consumers must then s
Details
Source
CPSC Consumer Product Recall
External ID
10360
Action Date
2025-07-24
Status
Recalled
Category
consumer_product
Product Description
This recall involves FENGQS F7 Pro electric bikes with batteries manufactured on April 21, 2024. The e-bikes were sold i
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.
Shenzhen Fengqisi Car Industry Co., Ltd., dba FENGQS, 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 (Shenzhen Fengqisi Car Industry Co., Ltd., dba FENGQS, 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 Shenzhen Fengqisi Car Industry Co., Ltd., dba FENGQS, of China have FDA actions?
Shenzhen Fengqisi Car Industry Co., Ltd., dba FENGQS, 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 "10360" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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