Harbor Breeze Belleisle Bay and Honeywell Rio Ceiling Fans
Zhongshan Kong Luen Wah Hoi Electric Appliance Co. Ltd., of China
Summary
CPSC recall: Harbor Breeze Belleisle Bay and Honeywell Rio Ceiling Fans. By Zhongshan Kong Luen Wah Hoi Electric Appliance Co. Ltd., of China. Hazard: The blades can detach from the fan while in use, posing an impact injury hazard to consumers.. Remedy: Consumers should immediately stop using the recalled fans and contact Hong Kong China Electric Appliance Manufacture Company ("HKC") to confirm their fan is under the scope of the recall by providing the firm a photo of the fan and date code. The
Details
Source
CPSC Consumer Product Recall
External ID
9188
Action Date
2021-12-15
Status
Recalled
Category
consumer_product
Product Description
This recall involves Harbor Breeze 52-inch Belleisle Bay and Honeywell 52-inch Rio ceiling fans, which are identical fan
Context & Analysis
This is a unclassified recall.
This was one of 6 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Zhongshan Kong Luen Wah Hoi Electric Appliance Co. Ltd., of China 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 (Zhongshan Kong Luen Wah Hoi Electric Appliance Co. Ltd., of China) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Zhongshan Kong Luen Wah Hoi Electric Appliance Co. Ltd., of China have FDA actions?
Zhongshan Kong Luen Wah Hoi Electric Appliance Co. Ltd., of China 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 "9188" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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