RecallHawk

Van Rysel GRVL AF Bicycles

Unknown Manufacturer

Summary

CPSC recalled Van Rysel GRVL AF Bicycles by Unknown Manufacturer. Hazard: The recalled bicycles’ front lock nut can loosen during use, causing the front wheel to dislodge or loosen over time, posing a crash hazard.. Remedy: Consumers should stop using the recalled bicycles immediately and take them to the nearest Recreational Equipment (REI Co-op) location for a free inspection and repair service of the front fork assembly. Anyone unable to visit an REI Co-op location can contact Decathlon Customer Service directly for assistance. Recalled models can be identified by the Van Rysel Product ID on the top right of the product label under the frame, beginning with the number 5..

Details

Source

cpsc

External ID

27017

Action Date

2026-10-08

Status

Ongoing

Category

product

Product Code

Bicycles or Accessories

Product Description

This recall involves adult multi-terrain gravel bicycles Van Rysel GRVL AF Sword Brown CN FR (model number 8911304), Van Rysel GRVL AF Apex Beige CN FR (model number 8911305), Van Rysel GRVL AF Sword Pink CN FR (model number 8911308), and Van Rysel GRVL AF GRX Black (model number 8929130). The recalled models were sold in sizes x-small, small, medium, large and x-large. The bicycles are designed for off-road gravel riding, road cycling, commuting and bikepacking. Each bicycle can be identified by the model name and Van Rysel Product ID located on the barcode sticker on the frame near the bottom bracket. Only Van Rysel bicycles with the following Product IDs/ SKUs are included in this recall.

Context & Analysis

Unknown Manufacturer has 1449 FDA actions in our database.

Frequently Asked Questions

How often does Unknown Manufacturer have FDA actions?

Unknown Manufacturer has 1449 FDA actions in our database, including 0 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.

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