MI 1615 and 1617 Sliding Glass Doors; Window World 4000 Series and 8000 Series Sliding Glass Doors
Summary
CPSC recall: 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 p
Details
Source
CPSC Consumer Product Recall
External ID
9768
Action Date
2023-11-22
Status
Recalled
Category
consumer_product
Product Description
This recall involves certain MI Windows and Doors 1615 and 1617 sliding glass doors (if sold as impact-resistant or with
Context & Analysis
This is a unclassified recall.
This was one of 9 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
MI Windows and Doors LLC, of Harrisburg, Pennsylvania has 4 FDA actions in our database, including 2 recalls.
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 (MI Windows and Doors LLC, of Harrisburg, Pennsylvania) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
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. Search for "9768" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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