Residential 300 Series Snow Blowers
Husqvarna Professional Products Inc., of Charlotte, North Carolina
Summary
CPSC recall: Residential 300 Series Snow Blowers. By Husqvarna Professional Products Inc., of Charlotte, North Carolina. Hazard: The recalled 300 series snow blowers can unexpectedly go into drive mode and collide with a consumer, posing an injury hazard.. Remedy: Consumers should immediately stop using the recalled snow blowers and contact an authorized Husqvarna Professional Products dealer for a free repair. The dealer locator is available at https://locations.husqvarna.com/us/..
Details
Source
CPSC Consumer Product Recall
External ID
9665
Action Date
2023-07-06
Status
Recalled
Category
consumer_product
Product Description
This recall involves Husqvarna-branded gas-powered residential 300 Series Snow Blowers with model numbers ST 324, ST 327
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.
Husqvarna Professional Products Inc., of Charlotte, North Carolina 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 (Husqvarna Professional Products Inc., of Charlotte, North Carolina) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Husqvarna Professional Products Inc., of Charlotte, North Carolina have FDA actions?
Husqvarna Professional Products Inc., of Charlotte, North Carolina 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 "9665" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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