RecallHawk

1620 vinyl single-hung impact windows with window opening control devices

MI Windows and Doors LLC, of Harrisburg, Pennsylvania

Summary

CPSC recall: 1620 vinyl single-hung impact windows with window opening control devices. By MI Windows and Doors LLC, of Harrisburg, Pennsylvania. Hazard: The tilt latch can cause the window opening control devices to malfunction, posing fall and serious injury hazards.. Remedy: Consumers should immediately close and lock the recalled windows and contact MI Windows and Doors for a free repair. MI will arrange for a free in-home repair to replace the window opening control devices. MI Windows and

Details

Source

CPSC Consumer Product Recall

External ID

9499

Action Date

2023-01-12

Status

Recalled

Category

consumer_product

Product Description

This recall involves the MI Windows and Doors 1620 vinyl single-hung impact windows with window opening control devices.

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 "9499" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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