Open Cycle UP Ekar, UPPER Ekar, WIDE Ekar and MIND Ekar bicycles
Summary
CPSC recall: Open Cycle UP Ekar, UPPER Ekar, WIDE Ekar and MIND Ekar bicycles. By Open Cycle AG, of Switzerland. Hazard: The rear brake can fail, posing a crash hazard.. Remedy: Consumers should immediately stop using the recalled bicycles and framesets and contact their local bicycle dealer to schedule free installation of the repair kit. The repair kit includes a hydraulic brake hose/line, and a new frame insert for the rear brake hose and rear shift cable..
Details
Source
CPSC Consumer Product Recall
External ID
9579
Action Date
2023-03-30
Status
Recalled
Category
consumer_product
Product Description
This recall involves Open Cycle-branded bicycles, models U.P. Ekar, UPPER Ekar, WIDE Ekar and MIND Ekar; and all Open Cy
Context & Analysis
This is a unclassified recall.
This was one of 12 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Open Cycle 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 (Open Cycle 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 Open Cycle AG, of Switzerland have FDA actions?
Open Cycle 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 "9579" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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