RecallHawk

Schwinn Tone Electric Scooters (e-scooters)

Mast Work Handicraft Co. Ltd., of China

Summary

CPSC recall: Schwinn Tone Electric Scooters (e-scooters). By Mast Work Handicraft Co. Ltd., of China. Hazard: The e-scooter's handlebar grips can loosen or crack, posing fall and injury hazards.. Remedy: Consumers should immediately stop using the recalled e-scooters and contact Pacific Cycle for a free repair kit. Consumers will need to provide the serial number of their scooter and a mailing address. The repair kit can be installed by the consumer and includes all required tools and instructio

Details

Source

CPSC Consumer Product Recall

External ID

9186

Action Date

2021-12-15

Status

Recalled

Category

consumer_product

Product Description

This recall involves all models of the Schwinn Tone Electric Scooter. That includes the Tone 1, Tone 2 and Tone 3 models

Context & Analysis

This is a unclassified recall.

This was one of 6 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Mast Work Handicraft Co. Ltd., of China 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 (Mast Work Handicraft Co. Ltd., of China) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Mast Work Handicraft Co. Ltd., of China have FDA actions?

Mast Work Handicraft Co. Ltd., of China 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 "9186" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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