RecallHawk

Model Year 2023 Yamaha Golf Car, Personal Transportation Vehicles (PTV) and Umax

Yamaha Motor Powered Products Co. LTD., of Japan

Summary

CPSC recall: Model Year 2023 Yamaha Golf Car, Personal Transportation Vehicles (PTV) and Umax. By Yamaha Motor Powered Products Co. LTD., of Japan. Hazard: The accelerator spring can become dislodged, allowing the accelerator pedal not to return to the resting position, posing crash and injury or death hazards.. Remedy: Consumers should immediately stop using the recalled 2023 Yamaha Golf Car, PTV and Umax and contact Yamaha for a free inspection and repair. Yamaha is contacting known purchasers

Details

Source

CPSC Consumer Product Recall

External ID

9666

Action Date

2023-07-06

Status

Recalled

Category

consumer_product

Product Description

This recall involves model year 2023 Golf Car and Personal Transportation vehicles. The vehicles were sold in various co

Context & Analysis

This is a unclassified recall.

This was one of 8 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Yamaha Motor Powered Products Co. LTD., of Japan 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 (Yamaha Motor Powered Products Co. LTD., of Japan) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Yamaha Motor Powered Products Co. LTD., of Japan have FDA actions?

Yamaha Motor Powered Products Co. LTD., of Japan 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 "9666" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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