MI 1615 and 1617 Sliding Glass Doors; Window World 4000 Series and 8000 Series Sliding Glass Doors
Summary
CPSC recalled MI 1615 and 1617 Sliding Glass Doors; Window World 4000 Series and 8000 Series Sliding Glass Doors by MI Windows and Doors LLC, of Harrisburg, Pennsylvania. Hazard: The glass can separate from the frame during hurricane conditions which can pose a serious injury hazard.. Remedy: Consumers should avoid areas with the recalled doors during hurricane conditions and contact MI Windows and Doors to schedule a free repair. Prior to repair, cover the doors with plywood or other suitable protection if a hurricane warning is issued for your location. MI Windows and Doors is contacting all known purchasers directly..
Details
Source
cpsc
External ID
24717
Action Date
2023-11-22
Status
Ongoing
Category
product
Product Description
This recall involves certain MI Windows and Doors 1615 and 1617 sliding glass doors (if sold as impact-resistant or with a DP50 upgrade), Window World 4000 Series sliding glass doors (with DP50 upgrade), and Window World 8000 Series sliding glass doors. The doors were sold in several colors and sizes with a variety of handle options. All recalled doors have an aluminum interlock and an LC-PG50 performance grade. The recalled impact doors have MTL-12 on the door label; recalled DP50 doors have MTL-12 or MTL-2. The door label located at the top of the window also has the manufacturer, series number, performance grade, and manufacture date (MFG: M/YYYY) on the label.
Context & Analysis
MI Windows and Doors LLC, of Harrisburg, Pennsylvania has 4 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
How often does MI Windows and Doors LLC, of Harrisburg, Pennsylvania have FDA actions?
MI Windows and Doors LLC, of Harrisburg, Pennsylvania has 4 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.
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