RecallHawk

Model Year 2020-2021 RANGER 1000, RANGER CREW 1000, RANGER XP 1000, and RANGER CREW XP 1000 and Model Year 2020 ProXD 20

Polaris Inc., of Medina, Minn.

Summary

CPSC recall: Model Year 2020-2021 RANGER 1000, RANGER CREW 1000, RANGER XP 1000, and RANGER CREW XP 1000 and Model Year 2020 ProXD 2000G, ProXD 2000G H, ProXD 4000G, and ProXD 4000G H. By Polaris Inc., of Medina, Minn.. Hazard: The throttle pedal can return to the idle position more slowly than anticipated once the pedal is released or stick in the depressed position, posing a crash hazard.. Remedy: Consumers should immediately stop using the recalled vehicles and contact a Polaris dealer to sch

Details

Source

CPSC Consumer Product Recall

External ID

9011

Action Date

2021-03-04

Status

Recalled

Category

consumer_product

Product Description

This recall involves Model Year 2020-2021 RANGER 1000, RANGER CREW 1000, RANGER XP 1000, and RANGER CREW XP 1000 recreat

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.

Polaris Inc., of Medina, Minn. has 6 FDA actions in our database, including 3 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 (Polaris Inc., of Medina, Minn.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Polaris Inc., of Medina, Minn. have FDA actions?

Polaris Inc., of Medina, Minn. has 6 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9011" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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