SIMU DMI6 Hz motors sold with awnings and shutters
Summary
CPSC recall: SIMU DMI6 Hz motors sold with awnings and shutters. By SIMU authorized dealers, installers and contractors from March 2018 through June 2022 with awnings or shutters for between $1,260 and $1,740.. Hazard: The awning and shutter motor's power cable can disconnect while opened or closed manually (using the manual override feature), posing electric shock and electrocution hazards.. Remedy: Consumers should immediately stop using the manual override feature if their motorized awnings o
Details
Source
CPSC Consumer Product Recall
External ID
9478
Action Date
2022-12-15
Status
Recalled
Category
consumer_product
Product Description
The recall involves SIMU DMI6 Hz Motors sold with and used to open and retract awnings and shutters. The motor is silver
Context & Analysis
This is a unclassified recall.
This was one of 14 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 (SIMU authorized dealers, installers and contractors from March 2018 through June 2022 with awnings or shutters for between $1,260 and $1,740.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does SIMU authorized dealers, installers and contractors from March 2018 through June 2022 with awnings or shutters for between $1,260 and $1,740. have FDA actions?
This is the only FDA action we have on record for SIMU authorized dealers, installers and contractors from March 2018 through June 2022 with awnings or shutters for between $1,260 and $1,740. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9478" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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