Knog Blinder 900 and Blinder 1300 Front Bicycle Lights
Summary
CPSC recall: Knog Blinder 900 and Blinder 1300 Front Bicycle Lights. By Independent bicycle retailers nationwide and online at Amazon between January 2023 and August 2025 for between $60 and $100.. Hazard: The lithium-ion battery in the bicycle light can overheat and catch fire, posing a risk of fire and burn hazards.. Remedy: Consumers should immediately stop using the recalled bicycle light and register at http://www.knog.com/recall for instructions on how to receive a free replacement bicycle
Details
Source
CPSC Consumer Product Recall
External ID
10452
Action Date
2025-10-30
Status
Recalled
Category
consumer_product
Product Description
This recall involves the Knog Blinder 900 and Blinder 1300 Front Bicycle Lights with the following batch codes: 0124AA,
Context & Analysis
This is a unclassified recall.
This was one of 25 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
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 (Independent bicycle retailers nationwide and online at Amazon between January 2023 and August 2025 for between $60 and $100.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Independent bicycle retailers nationwide and online at Amazon between January 2023 and August 2025 for between $60 and $100. have FDA actions?
This is the only FDA action we have on record for Independent bicycle retailers nationwide and online at Amazon between January 2023 and August 2025 for between $60 and $100. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10452" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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