RecallHawk

E-Z-GO Freedom RXV with Rear Facing Seat Personal Transportation Vehicles (PTV)

Textron Specialized Vehicles of Augusta, Georgia

Summary

CPSC recall: E-Z-GO Freedom RXV with Rear Facing Seat Personal Transportation Vehicles (PTV). By Textron Specialized Vehicles of Augusta, Georgia. Hazard: The rear seat structure of the PTV can fail, resulting in the rear seat tilting unexpectedly, posing fall and injury hazards to the riders.. Remedy: Consumers should immediately stop using the rear facing seat of their recalled vehicle and contact Textron for a free repair. Textron Specialized Vehicles is contacting all purchasers directly to

Details

Source

CPSC Consumer Product Recall

External ID

9209

Action Date

2022-01-13

Status

Recalled

Category

consumer_product

Product Description

This recall involves model-year 2022 E-Z-GO Freedom RXV ELiTE, Freedom RXV Gas, and Freedom RXV 48V personal transportat

Context & Analysis

This is a unclassified recall.

This was one of 9 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Textron Specialized Vehicles of Augusta, Georgia has 30 FDA actions in our database, including 15 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 (Textron Specialized Vehicles of Augusta, Georgia) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Textron Specialized Vehicles of Augusta, Georgia have FDA actions?

Textron Specialized Vehicles of Augusta, Georgia has 30 FDA actions in our database, including 15 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9209" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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