RecallHawk

Walk-Behind Leaf Blowers and Vacuums, and Tow-Behind Leaf Vacuums

Generac Power Systems Inc., of Waukesha, Wisconsin

Summary

CPSC recall: Walk-Behind Leaf Blowers and Vacuums, and Tow-Behind Leaf Vacuums. By Generac Power Systems Inc., of Waukesha, Wisconsin. Hazard: Pieces from the recalled leaf blowers and vacuums can come loose inside the unit and be ejected, posing a laceration hazard to users and bystanders.. Remedy: Consumers should immediately stop using the recalled leaf blowers and vacuums, and contact DR Power for a free dealer-installed repair..

Details

Source

CPSC Consumer Product Recall

External ID

9943

Action Date

2024-05-02

Status

Recalled

Category

consumer_product

Product Description

This recall involves DR Power Equipment walk-behind leaf blowers and vacuums, and tow-behind leaf vacuums with the follo

Context & Analysis

This is a unclassified recall.

This was one of 16 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Generac Power Systems Inc., of Waukesha, Wisconsin has 12 FDA actions in our database, including 6 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 (Generac Power Systems Inc., of Waukesha, Wisconsin) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Generac Power Systems Inc., of Waukesha, Wisconsin have FDA actions?

Generac Power Systems Inc., of Waukesha, Wisconsin has 12 FDA actions in our database, including 6 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9943" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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