RecallHawk

MI 1615 and 1617 Sliding Glass Doors; Window World 4000 Series and 8000 Series Sliding Glass Doors

MI Windows and Doors LLC, of Harrisburg, Pennsylvania

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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