Rossignol 2018 and 2019 Model Year All Track DH Bicycles
Rossignol dealers/rental resorts nationwide from March 2018 through October 2020 for about $3,800.
Summary
CPSC recall: Rossignol 2018 and 2019 Model Year All Track DH Bicycles. By Rossignol dealers/rental resorts nationwide from March 2018 through October 2020 for about $3,800.. Hazard: Cracks can form at the head tube area of the bicycle, where the fork connects to the bicycle. This can cause the frame to fail and allow the fork and front wheel to unexpectedly separate from the rest of the bicycle, posing a fall hazard to riders.. Remedy: Consumers should immediately stop using the recalled bicycle
Details
Source
CPSC Consumer Product Recall
External ID
9121
Action Date
2021-08-12
Status
Recalled
Category
consumer_product
Product Description
This recall includes Rossignol 2018 and 2019 model year All Track DH bicycles. The bicycle was produced in Matte Black (
Company
Context & Analysis
This is a unclassified recall.
This was one of 5 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 (Rossignol dealers/rental resorts nationwide from March 2018 through October 2020 for about $3,800.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Rossignol dealers/rental resorts nationwide from March 2018 through October 2020 for about $3,800. have FDA actions?
This is the only FDA action we have on record for Rossignol dealers/rental resorts nationwide from March 2018 through October 2020 for about $3,800. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9121" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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