RecallHawk

LiftMaster myQ Garage Door Control Panels

Grupo Chamberlain S.de R.L. de C.V., of Mexico

Summary

CPSC recall: LiftMaster myQ Garage Door Control Panels. By Grupo Chamberlain S.de R.L. de C.V., of Mexico. Hazard: The control panel's secondary entrapment protection system can fail causing the garage door to close even with an obstruction present, posing an entrapment hazard.. Remedy: Consumers should immediately contact the Chamberlain Group to receive a free repair kit, including shipping. The repair kit consists of a replacement garage door control panel and installation instructions. Insta

Details

Source

CPSC Consumer Product Recall

External ID

9526

Action Date

2023-02-09

Status

Recalled

Category

consumer_product

Product Description

This recall involves LiftMaster myQ garage door control panels, sold individually or with wall-mount residential jacksha

Context & Analysis

This is a unclassified recall.

This was one of 13 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Grupo Chamberlain S.de R.L. de C.V., of Mexico 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 (Grupo Chamberlain S.de R.L. de C.V., of Mexico) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Grupo Chamberlain S.de R.L. de C.V., of Mexico have FDA actions?

Grupo Chamberlain S.de R.L. de C.V., of Mexico 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 "9526" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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