Husqvarna Automower 435X and 535 All-Wheel Drive Robotic Lawnmowers
Summary
CPSC recall: Husqvarna Automower 435X and 535 All-Wheel Drive Robotic Lawnmowers. By Husqvarna affiliated dealers nationwide and online at www.husqvarna.com from March 2020 through July 2021 for about $4,500.. Hazard: The lithium-ion battery in the lawnmower can overheat, posing a risk of fire.. Remedy: Consumers should immediately stop using the recalled lawnmowers and download the free software update that Husqvarna Professional Products is pushing to the recalled units. Consumers with units h
Details
Source
CPSC Consumer Product Recall
External ID
9244
Action Date
2022-02-17
Status
Recalled
Category
consumer_product
Product Description
This recall involves the Husqvarna-branded Automower 435X AWD and Automower 535 AWD robotic lawnmowers, both of which ar
Context & Analysis
This is a unclassified recall.
This was one of 18 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
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 affiliated dealers nationwide and online at www.husqvarna.com from March 2020 through July 2021 for about $4,500.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Husqvarna affiliated dealers nationwide and online at www.husqvarna.com from March 2020 through July 2021 for about $4,500. have FDA actions?
This is the only FDA action we have on record for Husqvarna affiliated dealers nationwide and online at www.husqvarna.com from March 2020 through July 2021 for about $4,500. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9244" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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