RecallHawk

Hunter branded Devon Park, Astwood, Highland Hill, Kerrison and Van Nuys light fixtures

Unknown Manufacturer

Summary

CPSC recalled Hunter branded Devon Park, Astwood, Highland Hill, Kerrison and Van Nuys light fixtures by Unknown Manufacturer. Hazard: The internal wires in the lights can be damaged, posing an electric shock hazard to the consumer.. Remedy: Consumers should immediately stop using the recalled lighting products and contact Hunter to receive a full refund..

Details

Source

cpsc

External ID

23041

Action Date

2022-11-10

Status

Ongoing

Category

product

Product Description

This recall involves 41 models of Hunter lighting fixtures from the Devon Park, Astwood, Highland Hill, Kerrison, and Van Nuys lighting collections. The model number can be found on a label behind the light when removed from the wall. The lights were sold with single, 2, 3, 4 and 5-light fixtures and in various finishes including brushed and polished nickel, Onyx black, Alturas gold, Distressed white and rust. Lights included in the recall are listed below. To view photos of all recalled models, visit www.hunterfan.com/recall. Light Collection Description Model Devon Park Sconce 19143 19144 2 Light Vanity 19145 19146 3 Light Vanity 19147 19148 4 Light Vanity 19149 19150 Astwood 2 Light Vanity 19127 19128 19963 19964 3 Light Vanity 19129 19130 19965 19966 4 Light Vanity 19131 19132 19967 19968 5 Light Linear 19121 19122 19955 19956 Highland Hill Chandelier 19287 19288 19982 Kerrison 2 Light Vanity 19550 19551 3 Light Vanity 19552 19553 4 Light Vanity 19554 19555 Van Nuys 2 Light Vanity 19301 19302 3 Light Vanity 19303 19304 4 Light Vanity 19305 19306 4 Light Linear 19323 19324

Context & Analysis

Unknown Manufacturer has 1320 FDA actions in our database.

Frequently Asked Questions

How often does Unknown Manufacturer have FDA actions?

Unknown Manufacturer has 1320 FDA actions in our database, including 0 recalls 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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