RecallHawk

GreenSpeed Magnum and Magnum XL recumbent trikes with quick release front axles and replacement Quick Release Axles

WizWheelz Inc., of Grand Rapids, Michigan

Summary

CPSC recall: GreenSpeed Magnum and Magnum XL recumbent trikes with quick release front axles and replacement Quick Release Axles. By WizWheelz Inc., of Grand Rapids, Michigan. Hazard: The recalled recumbent trikes front axles were improperly assembled during manufacturing. The axles can come loose during use, causing the rider to lose control, posing crash and injury hazards.. Remedy: Consumers should immediately stop using the recalled trikes and return them to the place of purchase for a free

Details

Source

CPSC Consumer Product Recall

External ID

9302

Action Date

2022-05-05

Status

Recalled

Category

consumer_product

Product Description

This recall involves GreenSpeed Magnum and Magnum XL model recumbent trikes with Sturmey-Archer drum brake quick release

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.

WizWheelz Inc., of Grand Rapids, Michigan 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 (WizWheelz Inc., of Grand Rapids, Michigan) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does WizWheelz Inc., of Grand Rapids, Michigan have FDA actions?

WizWheelz Inc., of Grand Rapids, Michigan 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 "9302" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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