RecallHawk

Model Year 2021 GENERAL 1000, GENERAL 4 1000, GENERAL XP 1000 and GENERAL XP 4 1000 ROVs

Polaris Inc., of Medina, Minn.

Summary

CPSC recall: Model Year 2021 GENERAL 1000, GENERAL 4 1000, GENERAL XP 1000 and GENERAL XP 4 1000 ROVs. By Polaris Inc., of Medina, Minn.. Hazard: The weld between the brake pedal pivot bracket and the EPS mounting bracket can separate, which can result in a loss of brake function, posing a crash hazard.. Remedy: Consumers should immediately stop using the recalled vehicles and contact a Polaris dealer to schedule a free inspection and if needed, a free repair. Polaris is notifying dealers and co

Details

Source

CPSC Consumer Product Recall

External ID

9106

Action Date

2021-07-22

Status

Recalled

Category

consumer_product

Product Description

This recall involves Model Year 2021 GENERAL 1000, GENERAL 4 1000, GENERAL XP 1000, and GENERAL XP 4 1000 recreational o

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.

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 "9106" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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