Bella residential elevators
Bella Elevator, LLC, d/b/a Symmetry Elevating Solutions, of Peoria, Ill.
Summary
CPSC recall: Bella residential elevators. By Bella Elevator, LLC, d/b/a Symmetry Elevating Solutions, of Peoria, Ill.. Hazard: Young children can become entrapped in the space between the exterior landing (hoistway) door and the interior elevator car door or gate if there is a hazardous gap, and suffer serious injuries or death when the elevator is called to another floor.. Remedy: Consumers should keep unsupervised young children away from the recalled residential elevators and contact the manu
Details
Source
CPSC Consumer Product Recall
External ID
9203
Action Date
2022-01-11
Status
Recalled
Category
consumer_product
Product Description
This recall involves Bella residential elevators manufactured from 2009 to 2021. Models include Symmetry IGD, Hydraulic,
Context & Analysis
This is a unclassified recall.
This was one of 7 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Bella Elevator, LLC, d/b/a Symmetry Elevating Solutions, of Peoria, Ill. 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 (Bella Elevator, LLC, d/b/a Symmetry Elevating Solutions, of Peoria, Ill.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Bella Elevator, LLC, d/b/a Symmetry Elevating Solutions, of Peoria, Ill. have FDA actions?
Bella Elevator, LLC, d/b/a Symmetry Elevating Solutions, of Peoria, Ill. 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 "9203" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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