BMC-branded Kaius 01 bicycles and framesets
Summary
CPSC recall: BMC-branded Kaius 01 bicycles and framesets. By BMC Switzerland AG, of Switzerland. Hazard: The fork steerer tube on the recalled bicycles and framesets can crack, break, or separate during use, posing a fall hazard.. Remedy: Consumers should immediately stop using the recalled bicycles and contact an authorized BMC dealer for a free inspection and a free replacement of the forks. BMC is contacting all known purchasers directly..
Details
Source
CPSC Consumer Product Recall
External ID
10196
Action Date
2025-03-13
Status
Recalled
Category
consumer_product
Product Description
This recall involves all BMC-branded Kaius 01 bicycles and framesets. The bikes and framesets were sold in Peacock Spide
Context & Analysis
This is a unclassified recall.
This was one of 15 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
BMC Switzerland AG, of Switzerland 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 (BMC Switzerland AG, of Switzerland) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does BMC Switzerland AG, of Switzerland have FDA actions?
BMC Switzerland AG, of Switzerland 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 "10196" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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