RecallHawk

LG 86-inch smart televisions and stands

LG Electronics Reynosa, S.A. de C.V., of Reynosa, Mexico

Summary

CPSC recall: LG 86-inch smart televisions and stands. By LG Electronics Reynosa, S.A. de C.V., of Reynosa, Mexico. Hazard: The TV can become unstable while on the assembled stand, posing serious tip-over and entrapment hazards that can result in injuries or death to children and others.. Remedy: Consumers using the TV's supporting stand legs should immediately detach it and place the television in a safe location away from children. Contact LG Electronics for instructions on how to inspect the u

Details

Source

CPSC Consumer Product Recall

External ID

9498

Action Date

2023-01-12

Status

Recalled

Category

consumer_product

Product Description

This recall involves four LG Electronics 86-inch smart TV models with model numbers 86UQ8000AUB, 86UQ7070ZUD, 86UQ7590PU

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.

LG Electronics Reynosa, S.A. de C.V., of Reynosa, 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 (LG Electronics Reynosa, S.A. de C.V., of Reynosa, Mexico) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does LG Electronics Reynosa, S.A. de C.V., of Reynosa, Mexico have FDA actions?

LG Electronics Reynosa, S.A. de C.V., of Reynosa, 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 "9498" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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