American Landmaster EV, L3, L4, L5, L5W and L7 Utility Vehicles (UTVs)
Summary
CPSC recall: American Landmaster EV, L3, L4, L5, L5W and L7 Utility Vehicles (UTVs). By ASW LLC, d/b/a American Landmaster, of Columbia City, Ind.. Hazard: The steering shaft can separate from the joint and result in a loss of control, posing crash and injury hazards.. Remedy: Consumers should immediately stop using the recalled utility vehicles and contact American Landmaster to receive instructions for conducting an inspection to determine if your vehicle requires repair, or to make an appoint
Details
Source
CPSC Consumer Product Recall
External ID
9236
Action Date
2022-02-16
Status
Recalled
Category
consumer_product
Product Description
This recall involves American Landmaster utility vehicles series EV, L3, L4, L5, L5W and L7, equipped with standard (non
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.
ASW LLC, d/b/a American Landmaster, of Columbia City, Ind. 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 (ASW LLC, d/b/a American Landmaster, of Columbia City, Ind.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does ASW LLC, d/b/a American Landmaster, of Columbia City, Ind. have FDA actions?
ASW LLC, d/b/a American Landmaster, of Columbia City, Ind. 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 "9236" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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