Residential Elevators StrikeLock Hoistway Door Locking Device
Summary
CPSC recall: Residential Elevators StrikeLock Hoistway Door Locking Device. By Residential Elevators and authorized elevator dealers nationwide from April 2024 through March 2026 for about $1,000.. Hazard: The elevator's StrikeLock hoistway door locking device can allow the elevator cab to move with a landing door open, posing a risk of serious injury or death due to fall and injury hazards.. Remedy: Consumers should immediately stop using the residential elevator systems where StrikeLock hoistw
Details
Source
CPSC Consumer Product Recall
External ID
10747
Action Date
2026-04-30
Status
Recalled
Category
consumer_product
Product Description
This recall involves the StrikeLock hoistway door locking device, used to secure a residential elevator hoistway landing
Context & Analysis
This is a unclassified recall.
This was one of 26 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 (Residential Elevators and authorized elevator dealers nationwide from April 2024 through March 2026 for about $1,000.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Residential Elevators and authorized elevator dealers nationwide from April 2024 through March 2026 for about $1,000. have FDA actions?
This is the only FDA action we have on record for Residential Elevators and authorized elevator dealers nationwide from April 2024 through March 2026 for about $1,000. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10747" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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