Rear wheel bolts installed on model year 2026 Trek FX+ 1 and Electra Townie Go! electric bicycles
Summary
CPSC recalled Rear wheel bolts installed on model year 2026 Trek FX+ 1 and Electra Townie Go! electric bicycles by Hyena, Inc., of Taiwan. Hazard: The rear wheel bolts can break when torqued, causing the wheel to separate from the bicycle, posing a fall hazard.. Remedy: Consumers should immediately stop using the bicycles with recalled bolts and contact an authorized Trek or Electra dealer to schedule a free repair at the dealer's location. The dealer will replace the original black rear wheel bolts with new silver rear wheel bolts. Consumers can locate their nearest dealer at https://www.trekbikes.com./us/en_US/store-finder/. Trek will provide consumers who participate in the recall with a $10 in-store credit toward any Trek, Electra or Bontrager merchandise. The credit is valid through December 31, 2026..
Details
Source
cpsc
External ID
26220
Action Date
2026-01-29
Status
Ongoing
Category
product
Product Description
This recall involves the rear wheel bolts on model year 2026 Trek-branded FX+ 1 Midstep, FX+ 1S Midstep, FX+ 1 Stepover, and FX+ 1S Stepover, and Electra-branded Townie Go! Step Thru and Townie Go! S Step Thru electric bicycles sold before October 28, 2025. The bicycles come in various colors and sizes. The Trek bicycles have the word "TREK" printed on the downtube of the frame and "FX+" is printed on the top tube. The Electra bicycles have the word "townie" printed on the downtube, "electra" on the seat stay, and "go!" on the chain guard. The original rear wheel bolts are black and connect the motor to the rear frame of the bicycles.
Company
Context & Analysis
Hyena, Inc., of Taiwan has 2 FDA actions in our database, including 1 recall.
Frequently Asked Questions
How often does Hyena, Inc., of Taiwan have FDA actions?
Hyena, Inc., of Taiwan 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. 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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