RecallHawk

Ariens® DELUXE-, PLATINUM- and PROFESSIONAL-series Snow Throwers

Ariens Company, of Brillion, Wisconsin

Summary

CPSC recall: Ariens® DELUXE-, PLATINUM- and PROFESSIONAL-series Snow Throwers. By Ariens Company, of Brillion, Wisconsin. Hazard: The recalled snow thrower impeller and auger assembly can continue rotating even after the operator control lever is released, posing a laceration hazard if a user makes contact with the rotating parts inside the housing enclosure at the front of the machine.. Remedy: Consumers should immediately stop using the recalled snow throwers and contact Ariens Company or an a

Details

Source

CPSC Consumer Product Recall

External ID

10150

Action Date

2025-02-06

Status

Recalled

Category

consumer_product

Product Description

This recall involves certain Ariens DELUXE-, PLATINUM- and PROFESSIONAL-series Sno-Thro® models. The recalled snow throw

Context & Analysis

This is a unclassified recall.

This was one of 17 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Ariens Company, of Brillion, Wisconsin has 2 FDA actions in our database, including 1 recall.

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 (Ariens Company, of Brillion, Wisconsin) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Ariens Company, of Brillion, Wisconsin have FDA actions?

Ariens Company, of Brillion, Wisconsin has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10150" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for consumer_product

Related Actions