RecallHawk

Havertys Concord Dual Power Recliner Chairs

Artistic Leathers S de RL de CV, of Mexico (Chairs)

Summary

CPSC recall: Havertys Concord Dual Power Recliner Chairs. By Artistic Leathers S de RL de CV, of Mexico (Chairs). Hazard: When the chair is reclined and weight is applied to the chair back while returning to the upright position, the metal power mechanism assembly can bend, and cause the chair back to detach, posing a fall hazard to consumers.. Remedy: Consumers should immediately stop using the recalled recliner chairs and contact Havertys for a free repair by a service technician to install a

Details

Source

CPSC Consumer Product Recall

External ID

9657

Action Date

2023-06-22

Status

Recalled

Category

consumer_product

Product Description

This recall involves Havertys Concord Dual Power Recliner chairs with SKU 0-3500-1827 that is printed on a label affixed

Context & Analysis

This is a unclassified recall.

This was one of 10 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Artistic Leathers S de RL de CV, of Mexico (Chairs) 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 (Artistic Leathers S de RL de CV, of Mexico (Chairs)) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Artistic Leathers S de RL de CV, of Mexico (Chairs) have FDA actions?

Artistic Leathers S de RL de CV, of Mexico (Chairs) 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 "9657" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for consumer_product

Related Actions