SUNS SS6291 Solenoid Interlock Switches
Summary
CPSC recall: SUNS SS6291 Solenoid Interlock Switches. By SUNS International and authorized residential elevator dealers nationwide from September 2024 through November 2025 for about $200.. Hazard: The affected interlock switches can become stuck in a retracted position, allowing the exterior door to remain unlocked, posing a risk of death or serious injury if the elevator is called to another floor.. Remedy: Consumers should stop using their residential elevator containing the SUNS interlock sw
Details
Source
CPSC Consumer Product Recall
External ID
10804
Action Date
2026-06-04
Status
Recalled
Category
consumer_product
Product Description
This recall involves all SUNS International SS6291 Solenoid Interlock switches used in residential elevators produced fr
Context & Analysis
This is a unclassified recall.
This was one of 19 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 (SUNS International and authorized residential elevator dealers nationwide from September 2024 through November 2025 for about $200.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does SUNS International and authorized residential elevator dealers nationwide from September 2024 through November 2025 for about $200. have FDA actions?
This is the only FDA action we have on record for SUNS International and authorized residential elevator dealers nationwide from September 2024 through November 2025 for about $200. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10804" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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