RecallHawk

LiftMaster myQ Garage Door Control Panels

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

Summary

CPSC recalled 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. Installation instructions can also be found at https://support.chamberlaingroup.com. Chamberlain Group is contacting all known purchasers directly..

Details

Source

cpsc

External ID

23725

Action Date

2023-02-09

Status

Ongoing

Category

product

Product Description

This recall involves LiftMaster myQ garage door control panels, sold individually or with wall-mount residential jackshaft garage door openers. LiftMaster and myQ are printed on the front of the black control panels. The recalled control panels were manufactured between March 2022 and October 2022. The manufacture date, in MM/YY format, the model number and the UPC code are printed on a label located on the back of the unit. The following are the model numbers and UPC codes included in this recall: Model Numbers UPC Codes 8500MC 012381203536 8500CMC 012381203529 8500RGDMC 012381203543 RJO20MC 012381188246 RJO20CMC 012381191277 RJO20CHMC 012381191277 889LMMC 012381203611 889RGDMC 012381203628 041A7928-3MC 012381204304

Context & Analysis

Grupo Chamberlain S.de R.L. de C.V., of Mexico has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

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. 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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