Houoto 642-2150V Pool Drain Covers
Foshan Nanhai District Haichen Tengfei Hardware Factory, of China
Summary
CPSC recall: Houoto 642-2150V Pool Drain Covers. By Foshan Nanhai District Haichen Tengfei Hardware Factory, of China. Hazard: The drain covers do not bear the required product markings, in violation of the mandatory safety standard under the?Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing risk of serious injury or death from entrapment and drowning hazards. The drain covers also fail to meet safety requirements because they are missing statements regarding the service life of the c
Details
Source
CPSC Consumer Product Recall
External ID
10819
Action Date
2026-06-11
Status
Recalled
Category
consumer_product
Product Description
This recall involves Houoto 642-2150V Pool Drain Covers that are sold for use in swimming pools. The drain covers measur
Context & Analysis
This is a unclassified recall.
This was one of 25 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Foshan Nanhai District Haichen Tengfei Hardware Factory, 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 (Foshan Nanhai District Haichen Tengfei Hardware Factory, 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 Foshan Nanhai District Haichen Tengfei Hardware Factory, of China have FDA actions?
Foshan Nanhai District Haichen Tengfei Hardware Factory, 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 "10819" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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