GOETAS Pool Drain Covers
GuangZhouShiYiYangKangTiSheBeiYouXianGongSi, dba GOETAS, of China
Summary
CPSC recall: GOETAS Pool Drain Covers. By GuangZhouShiYiYangKangTiSheBeiYouXianGongSi, dba GOETAS, of China. Hazard: The recalled drain covers do not conform to the entrapment protection regulations of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing an entrapment hazard to swimmers and bathers.. Remedy: Pool owners/operators and consumers should immediately stop using pools with the recalled pool drain cover; and remove, replace and dispose of the recalled drain covers. Take a p
Details
Source
CPSC Consumer Product Recall
External ID
10048
Action Date
2024-09-12
Status
Recalled
Category
consumer_product
Product Description
This recall involves GOETAS-branded drain covers that are sold for use in swimming pools. The white, plastic, main pool
Context & Analysis
This is a unclassified recall.
This was one of 8 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
GuangZhouShiYiYangKangTiSheBeiYouXianGongSi, dba GOETAS, 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 (GuangZhouShiYiYangKangTiSheBeiYouXianGongSi, dba GOETAS, 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 GuangZhouShiYiYangKangTiSheBeiYouXianGongSi, dba GOETAS, of China have FDA actions?
GuangZhouShiYiYangKangTiSheBeiYouXianGongSi, dba GOETAS, 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 "10048" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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