RecallHawk

Footpads for Onewheel GT Electric Skateboards

Future Motion Inc., of Santa Cruz, California

Summary

CPSC recall: Footpads for Onewheel GT Electric Skateboards. By Future Motion Inc., of Santa Cruz, California. Hazard: The footpad can fail to disengage after the rider has dismounted while the board is in motion and the skateboard can unexpectedly continue to operate, posing an injury hazard to bystanders.. Remedy: Consumers should immediately stop using the skateboards with recalled footpads and contact Future Motion to determine whether their footpad is affected. Consumers with affected footpa

Details

Source

CPSC Consumer Product Recall

External ID

9371

Action Date

2022-08-11

Status

Recalled

Category

consumer_product

Product Description

This recall involves front footpads for Future Motion's Onewheel GT self-balancing electric skateboards, sold with the s

Context & Analysis

This is a unclassified recall.

This was one of 4 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Future Motion Inc., of Santa Cruz, California has 4 FDA actions in our database, including 2 recalls.

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 (Future Motion Inc., of Santa Cruz, California) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Future Motion Inc., of Santa Cruz, California have FDA actions?

Future Motion Inc., of Santa Cruz, California has 4 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9371" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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